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nsv5663666

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 327 SVs from 47 studies. See in: genome view    
Submitted genomic84,479,390-84,479,390Question Mark
Overlapping variant regions from other studies: 327 SVs from 47 studies. See in: genome view    
Remapped(Score: Perfect):84,512,996-84,512,996Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5663666Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1684,479,39084,479,390
nsv5663666RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1684,512,99684,512,996

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17088597insertionHG03065SequencingSequence alignment3,836
nssv17093141insertionSAMN00001694SequencingSequence alignment8,610

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17088597Submitted genomicNC_000016.10:g.844
79390_84479391ins1
34
GRCh38 (hg38)NC_000016.10Chr1684,479,39084,479,390
nssv17093141Submitted genomicNC_000016.10:g.844
79390_84479391ins5
8
GRCh38 (hg38)NC_000016.10Chr1684,479,39084,479,390
nssv17088597RemappedPerfectNC_000016.9:g.8451
2996_84512997ins13
4
GRCh37.p13First PassNC_000016.9Chr1684,512,99684,512,996
nssv17093141RemappedPerfectNC_000016.9:g.8451
2996_84512997ins58
GRCh37.p13First PassNC_000016.9Chr1684,512,99684,512,996

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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