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nsv517643

  • Variant Calls:22
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:42,573

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 704 SVs from 69 studies. See in: genome view    
Remapped(Score: Perfect):88,713,767-88,756,339Question Mark
Overlapping variant regions from other studies: 704 SVs from 69 studies. See in: genome view    
Remapped(Score: Perfect):88,780,175-88,822,747Question Mark
Overlapping variant regions from other studies: 9 SVs from 5 studies. See in: genome view    
Submitted genomic87,307,676-87,350,248Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv517643RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1688,713,76788,756,339
nsv517643RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1688,780,17588,822,747
nsv517643Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000016.8Chr1687,307,67687,350,248

Variant Call Information

Variant Call IDTypeMethodAnalysisZygosity
nssv691871copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv669932copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv691475copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv675166copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv689646copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv692965copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv652657copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv663521copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv665584copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv668671copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv681715copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv687496copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv688908copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv690237copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv672984copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv660783copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv664140copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv669113copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv673024copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv677150copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv677918copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv683672copy number lossSNP arraySNP genotyping analysisHeterozygous

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv691871RemappedPerfectNC_000016.10:g.(?_
88713767)_(8873877
5_?)del
GRCh38.p12First PassNC_000016.10Chr1688,713,76788,738,775
nssv669932RemappedPerfectNC_000016.10:g.(?_
88713767)_(8874079
7_?)del
GRCh38.p12First PassNC_000016.10Chr1688,713,76788,740,797
nssv691475RemappedPerfectNC_000016.10:g.(?_
88713767)_(8874079
7_?)del
GRCh38.p12First PassNC_000016.10Chr1688,713,76788,740,797
nssv675166RemappedPerfectNC_000016.10:g.(?_
88713767)_(8875599
3_?)del
GRCh38.p12First PassNC_000016.10Chr1688,713,76788,755,993
nssv689646RemappedPerfectNC_000016.10:g.(?_
88713767)_(8875599
3_?)del
GRCh38.p12First PassNC_000016.10Chr1688,713,76788,755,993
nssv692965RemappedPerfectNC_000016.10:g.(?_
88713767)_(8875633
9_?)del
GRCh38.p12First PassNC_000016.10Chr1688,713,76788,756,339
nssv652657RemappedPerfectNC_000016.10:g.(?_
88714632)_(8872750
2_?)del
GRCh38.p12First PassNC_000016.10Chr1688,714,63288,727,502
nssv663521RemappedPerfectNC_000016.10:g.(?_
88714632)_(8872750
2_?)del
GRCh38.p12First PassNC_000016.10Chr1688,714,63288,727,502
nssv665584RemappedPerfectNC_000016.10:g.(?_
88714632)_(8872750
2_?)del
GRCh38.p12First PassNC_000016.10Chr1688,714,63288,727,502
nssv668671RemappedPerfectNC_000016.10:g.(?_
88714632)_(8872750
2_?)del
GRCh38.p12First PassNC_000016.10Chr1688,714,63288,727,502
nssv681715RemappedPerfectNC_000016.10:g.(?_
88714632)_(8872750
2_?)del
GRCh38.p12First PassNC_000016.10Chr1688,714,63288,727,502
nssv687496RemappedPerfectNC_000016.10:g.(?_
88714632)_(8872750
2_?)del
GRCh38.p12First PassNC_000016.10Chr1688,714,63288,727,502
nssv688908RemappedPerfectNC_000016.10:g.(?_
88714632)_(8872750
2_?)del
GRCh38.p12First PassNC_000016.10Chr1688,714,63288,727,502
nssv690237RemappedPerfectNC_000016.10:g.(?_
88714632)_(8872750
2_?)del
GRCh38.p12First PassNC_000016.10Chr1688,714,63288,727,502
nssv672984RemappedPerfectNC_000016.10:g.(?_
88714632)_(8874079
7_?)del
GRCh38.p12First PassNC_000016.10Chr1688,714,63288,740,797
nssv660783RemappedPerfectNC_000016.10:g.(?_
88716268)_(8872750
2_?)del
GRCh38.p12First PassNC_000016.10Chr1688,716,26888,727,502
nssv664140RemappedPerfectNC_000016.10:g.(?_
88716268)_(8872750
2_?)del
GRCh38.p12First PassNC_000016.10Chr1688,716,26888,727,502
nssv669113RemappedPerfectNC_000016.10:g.(?_
88716268)_(8872750
2_?)del
GRCh38.p12First PassNC_000016.10Chr1688,716,26888,727,502
nssv673024RemappedPerfectNC_000016.10:g.(?_
88716268)_(8872750
2_?)del
GRCh38.p12First PassNC_000016.10Chr1688,716,26888,727,502
nssv677150RemappedPerfectNC_000016.10:g.(?_
88716268)_(8872750
2_?)del
GRCh38.p12First PassNC_000016.10Chr1688,716,26888,727,502
nssv677918RemappedPerfectNC_000016.10:g.(?_
88716268)_(8872750
2_?)del
GRCh38.p12First PassNC_000016.10Chr1688,716,26888,727,502
nssv683672RemappedPerfectNC_000016.10:g.(?_
88716268)_(8872750
2_?)del
GRCh38.p12First PassNC_000016.10Chr1688,716,26888,727,502
nssv691871RemappedPerfectNC_000016.9:g.(?_8
8780175)_(88805183
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,780,17588,805,183
nssv669932RemappedPerfectNC_000016.9:g.(?_8
8780175)_(88807205
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,780,17588,807,205
nssv691475RemappedPerfectNC_000016.9:g.(?_8
8780175)_(88807205
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,780,17588,807,205
nssv675166RemappedPerfectNC_000016.9:g.(?_8
8780175)_(88822401
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,780,17588,822,401
nssv689646RemappedPerfectNC_000016.9:g.(?_8
8780175)_(88822401
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,780,17588,822,401
nssv692965RemappedPerfectNC_000016.9:g.(?_8
8780175)_(88822747
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,780,17588,822,747
nssv652657RemappedPerfectNC_000016.9:g.(?_8
8781040)_(88793910
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,781,04088,793,910
nssv663521RemappedPerfectNC_000016.9:g.(?_8
8781040)_(88793910
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,781,04088,793,910
nssv665584RemappedPerfectNC_000016.9:g.(?_8
8781040)_(88793910
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,781,04088,793,910
nssv668671RemappedPerfectNC_000016.9:g.(?_8
8781040)_(88793910
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,781,04088,793,910
nssv681715RemappedPerfectNC_000016.9:g.(?_8
8781040)_(88793910
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,781,04088,793,910
nssv687496RemappedPerfectNC_000016.9:g.(?_8
8781040)_(88793910
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,781,04088,793,910
nssv688908RemappedPerfectNC_000016.9:g.(?_8
8781040)_(88793910
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,781,04088,793,910
nssv690237RemappedPerfectNC_000016.9:g.(?_8
8781040)_(88793910
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,781,04088,793,910
nssv672984RemappedPerfectNC_000016.9:g.(?_8
8781040)_(88807205
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,781,04088,807,205
nssv660783RemappedPerfectNC_000016.9:g.(?_8
8782676)_(88793910
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,782,67688,793,910
nssv664140RemappedPerfectNC_000016.9:g.(?_8
8782676)_(88793910
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,782,67688,793,910
nssv669113RemappedPerfectNC_000016.9:g.(?_8
8782676)_(88793910
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,782,67688,793,910
nssv673024RemappedPerfectNC_000016.9:g.(?_8
8782676)_(88793910
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,782,67688,793,910
nssv677150RemappedPerfectNC_000016.9:g.(?_8
8782676)_(88793910
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,782,67688,793,910
nssv677918RemappedPerfectNC_000016.9:g.(?_8
8782676)_(88793910
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,782,67688,793,910
nssv683672RemappedPerfectNC_000016.9:g.(?_8
8782676)_(88793910
_?)del
GRCh37.p13First PassNC_000016.9Chr1688,782,67688,793,910
nssv691871Submitted genomicNC_000016.8:g.(?_8
7307676)_(87332684
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,307,67687,332,684
nssv669932Submitted genomicNC_000016.8:g.(?_8
7307676)_(87334706
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,307,67687,334,706
nssv691475Submitted genomicNC_000016.8:g.(?_8
7307676)_(87334706
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,307,67687,334,706
nssv675166Submitted genomicNC_000016.8:g.(?_8
7307676)_(87349902
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,307,67687,349,902
nssv689646Submitted genomicNC_000016.8:g.(?_8
7307676)_(87349902
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,307,67687,349,902
nssv692965Submitted genomicNC_000016.8:g.(?_8
7307676)_(87350248
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,307,67687,350,248
nssv652657Submitted genomicNC_000016.8:g.(?_8
7308541)_(87321411
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,308,54187,321,411
nssv663521Submitted genomicNC_000016.8:g.(?_8
7308541)_(87321411
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,308,54187,321,411
nssv665584Submitted genomicNC_000016.8:g.(?_8
7308541)_(87321411
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,308,54187,321,411
nssv668671Submitted genomicNC_000016.8:g.(?_8
7308541)_(87321411
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,308,54187,321,411
nssv681715Submitted genomicNC_000016.8:g.(?_8
7308541)_(87321411
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,308,54187,321,411
nssv687496Submitted genomicNC_000016.8:g.(?_8
7308541)_(87321411
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,308,54187,321,411
nssv688908Submitted genomicNC_000016.8:g.(?_8
7308541)_(87321411
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,308,54187,321,411
nssv690237Submitted genomicNC_000016.8:g.(?_8
7308541)_(87321411
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,308,54187,321,411
nssv672984Submitted genomicNC_000016.8:g.(?_8
7308541)_(87334706
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,308,54187,334,706
nssv660783Submitted genomicNC_000016.8:g.(?_8
7310177)_(87321411
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,310,17787,321,411
nssv664140Submitted genomicNC_000016.8:g.(?_8
7310177)_(87321411
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,310,17787,321,411
nssv669113Submitted genomicNC_000016.8:g.(?_8
7310177)_(87321411
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,310,17787,321,411
nssv673024Submitted genomicNC_000016.8:g.(?_8
7310177)_(87321411
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,310,17787,321,411
nssv677150Submitted genomicNC_000016.8:g.(?_8
7310177)_(87321411
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,310,17787,321,411
nssv677918Submitted genomicNC_000016.8:g.(?_8
7310177)_(87321411
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,310,17787,321,411
nssv683672Submitted genomicNC_000016.8:g.(?_8
7310177)_(87321411
_?)del
NCBI35 (hg17)NC_000016.8Chr1687,310,17787,321,411

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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