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nsv831489

  • Variant Calls:16
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:201,887

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1593 SVs from 85 studies. See in: genome view    
Remapped(Score: Good):144,342,140-144,544,026Question Mark
Overlapping variant regions from other studies: 1523 SVs from 85 studies. See in: genome view    
Remapped(Score: Perfect):145,565,802-145,769,410Question Mark
Overlapping variant regions from other studies: 35 SVs from 6 studies. See in: genome view    
Submitted genomic145,536,610-145,740,218Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv831489RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8144,342,140144,544,026
nsv831489RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8145,565,802145,769,410
nsv831489Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000008.9Chr8145,536,610145,740,218

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1447519copy number lossBAC aCGHProbe signal intensity
nssv1447520copy number lossBAC aCGHProbe signal intensity
nssv1447521copy number lossBAC aCGHProbe signal intensity
nssv1447522copy number lossBAC aCGHProbe signal intensity
nssv1447523copy number lossBAC aCGHProbe signal intensity
nssv1447524copy number lossBAC aCGHProbe signal intensity
nssv1447525copy number lossBAC aCGHProbe signal intensity
nssv1447526copy number lossBAC aCGHProbe signal intensity
nssv1447527copy number lossBAC aCGHProbe signal intensity
nssv1447528copy number lossBAC aCGHProbe signal intensity
nssv1447530copy number lossBAC aCGHProbe signal intensity
nssv1447531copy number lossBAC aCGHProbe signal intensity
nssv1447532copy number lossBAC aCGHProbe signal intensity
nssv1447533copy number lossBAC aCGHProbe signal intensity
nssv1447534copy number lossBAC aCGHProbe signal intensity
nssv1447535copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1447519RemappedGoodNC_000008.11:g.(14
4342140_?)_(?_1445
44026)del
GRCh38.p12First PassNC_000008.11Chr8144,342,140144,544,026
nssv1447520RemappedGoodNC_000008.11:g.(14
4342140_?)_(?_1445
44026)del
GRCh38.p12First PassNC_000008.11Chr8144,342,140144,544,026
nssv1447521RemappedGoodNC_000008.11:g.(14
4342140_?)_(?_1445
44026)del
GRCh38.p12First PassNC_000008.11Chr8144,342,140144,544,026
nssv1447522RemappedGoodNC_000008.11:g.(14
4342140_?)_(?_1445
44026)del
GRCh38.p12First PassNC_000008.11Chr8144,342,140144,544,026
nssv1447523RemappedGoodNC_000008.11:g.(14
4342140_?)_(?_1445
44026)del
GRCh38.p12First PassNC_000008.11Chr8144,342,140144,544,026
nssv1447524RemappedGoodNC_000008.11:g.(14
4342140_?)_(?_1445
44026)del
GRCh38.p12First PassNC_000008.11Chr8144,342,140144,544,026
nssv1447525RemappedGoodNC_000008.11:g.(14
4342140_?)_(?_1445
44026)del
GRCh38.p12First PassNC_000008.11Chr8144,342,140144,544,026
nssv1447526RemappedGoodNC_000008.11:g.(14
4342140_?)_(?_1445
44026)del
GRCh38.p12First PassNC_000008.11Chr8144,342,140144,544,026
nssv1447527RemappedGoodNC_000008.11:g.(14
4342140_?)_(?_1445
44026)del
GRCh38.p12First PassNC_000008.11Chr8144,342,140144,544,026
nssv1447528RemappedGoodNC_000008.11:g.(14
4342140_?)_(?_1445
44026)del
GRCh38.p12First PassNC_000008.11Chr8144,342,140144,544,026
nssv1447530RemappedGoodNC_000008.11:g.(14
4342140_?)_(?_1445
44026)del
GRCh38.p12First PassNC_000008.11Chr8144,342,140144,544,026
nssv1447531RemappedGoodNC_000008.11:g.(14
4342140_?)_(?_1445
44026)del
GRCh38.p12First PassNC_000008.11Chr8144,342,140144,544,026
nssv1447532RemappedGoodNC_000008.11:g.(14
4342140_?)_(?_1445
44026)del
GRCh38.p12First PassNC_000008.11Chr8144,342,140144,544,026
nssv1447533RemappedGoodNC_000008.11:g.(14
4342140_?)_(?_1445
44026)del
GRCh38.p12First PassNC_000008.11Chr8144,342,140144,544,026
nssv1447534RemappedGoodNC_000008.11:g.(14
4342140_?)_(?_1445
44026)del
GRCh38.p12First PassNC_000008.11Chr8144,342,140144,544,026
nssv1447535RemappedGoodNC_000008.11:g.(14
4342140_?)_(?_1445
44026)del
GRCh38.p12First PassNC_000008.11Chr8144,342,140144,544,026
nssv1447519RemappedPerfectNC_000008.10:g.(14
5565802_?)_(?_1457
69410)del
GRCh37.p13First PassNC_000008.10Chr8145,565,802145,769,410
nssv1447520RemappedPerfectNC_000008.10:g.(14
5565802_?)_(?_1457
69410)del
GRCh37.p13First PassNC_000008.10Chr8145,565,802145,769,410
nssv1447521RemappedPerfectNC_000008.10:g.(14
5565802_?)_(?_1457
69410)del
GRCh37.p13First PassNC_000008.10Chr8145,565,802145,769,410
nssv1447522RemappedPerfectNC_000008.10:g.(14
5565802_?)_(?_1457
69410)del
GRCh37.p13First PassNC_000008.10Chr8145,565,802145,769,410
nssv1447523RemappedPerfectNC_000008.10:g.(14
5565802_?)_(?_1457
69410)del
GRCh37.p13First PassNC_000008.10Chr8145,565,802145,769,410
nssv1447524RemappedPerfectNC_000008.10:g.(14
5565802_?)_(?_1457
69410)del
GRCh37.p13First PassNC_000008.10Chr8145,565,802145,769,410
nssv1447525RemappedPerfectNC_000008.10:g.(14
5565802_?)_(?_1457
69410)del
GRCh37.p13First PassNC_000008.10Chr8145,565,802145,769,410
nssv1447526RemappedPerfectNC_000008.10:g.(14
5565802_?)_(?_1457
69410)del
GRCh37.p13First PassNC_000008.10Chr8145,565,802145,769,410
nssv1447527RemappedPerfectNC_000008.10:g.(14
5565802_?)_(?_1457
69410)del
GRCh37.p13First PassNC_000008.10Chr8145,565,802145,769,410
nssv1447528RemappedPerfectNC_000008.10:g.(14
5565802_?)_(?_1457
69410)del
GRCh37.p13First PassNC_000008.10Chr8145,565,802145,769,410
nssv1447530RemappedPerfectNC_000008.10:g.(14
5565802_?)_(?_1457
69410)del
GRCh37.p13First PassNC_000008.10Chr8145,565,802145,769,410
nssv1447531RemappedPerfectNC_000008.10:g.(14
5565802_?)_(?_1457
69410)del
GRCh37.p13First PassNC_000008.10Chr8145,565,802145,769,410
nssv1447532RemappedPerfectNC_000008.10:g.(14
5565802_?)_(?_1457
69410)del
GRCh37.p13First PassNC_000008.10Chr8145,565,802145,769,410
nssv1447533RemappedPerfectNC_000008.10:g.(14
5565802_?)_(?_1457
69410)del
GRCh37.p13First PassNC_000008.10Chr8145,565,802145,769,410
nssv1447534RemappedPerfectNC_000008.10:g.(14
5565802_?)_(?_1457
69410)del
GRCh37.p13First PassNC_000008.10Chr8145,565,802145,769,410
nssv1447535RemappedPerfectNC_000008.10:g.(14
5565802_?)_(?_1457
69410)del
GRCh37.p13First PassNC_000008.10Chr8145,565,802145,769,410
nssv1447519Submitted genomicNC_000008.9:g.(145
536610_?)_(?_14574
0218)del
NCBI35 (hg17)NC_000008.9Chr8145,536,610145,740,218
nssv1447520Submitted genomicNC_000008.9:g.(145
536610_?)_(?_14574
0218)del
NCBI35 (hg17)NC_000008.9Chr8145,536,610145,740,218
nssv1447521Submitted genomicNC_000008.9:g.(145
536610_?)_(?_14574
0218)del
NCBI35 (hg17)NC_000008.9Chr8145,536,610145,740,218
nssv1447522Submitted genomicNC_000008.9:g.(145
536610_?)_(?_14574
0218)del
NCBI35 (hg17)NC_000008.9Chr8145,536,610145,740,218
nssv1447523Submitted genomicNC_000008.9:g.(145
536610_?)_(?_14574
0218)del
NCBI35 (hg17)NC_000008.9Chr8145,536,610145,740,218
nssv1447524Submitted genomicNC_000008.9:g.(145
536610_?)_(?_14574
0218)del
NCBI35 (hg17)NC_000008.9Chr8145,536,610145,740,218
nssv1447525Submitted genomicNC_000008.9:g.(145
536610_?)_(?_14574
0218)del
NCBI35 (hg17)NC_000008.9Chr8145,536,610145,740,218
nssv1447526Submitted genomicNC_000008.9:g.(145
536610_?)_(?_14574
0218)del
NCBI35 (hg17)NC_000008.9Chr8145,536,610145,740,218
nssv1447527Submitted genomicNC_000008.9:g.(145
536610_?)_(?_14574
0218)del
NCBI35 (hg17)NC_000008.9Chr8145,536,610145,740,218
nssv1447528Submitted genomicNC_000008.9:g.(145
536610_?)_(?_14574
0218)del
NCBI35 (hg17)NC_000008.9Chr8145,536,610145,740,218
nssv1447530Submitted genomicNC_000008.9:g.(145
536610_?)_(?_14574
0218)del
NCBI35 (hg17)NC_000008.9Chr8145,536,610145,740,218
nssv1447531Submitted genomicNC_000008.9:g.(145
536610_?)_(?_14574
0218)del
NCBI35 (hg17)NC_000008.9Chr8145,536,610145,740,218
nssv1447532Submitted genomicNC_000008.9:g.(145
536610_?)_(?_14574
0218)del
NCBI35 (hg17)NC_000008.9Chr8145,536,610145,740,218
nssv1447533Submitted genomicNC_000008.9:g.(145
536610_?)_(?_14574
0218)del
NCBI35 (hg17)NC_000008.9Chr8145,536,610145,740,218
nssv1447534Submitted genomicNC_000008.9:g.(145
536610_?)_(?_14574
0218)del
NCBI35 (hg17)NC_000008.9Chr8145,536,610145,740,218
nssv1447535Submitted genomicNC_000008.9:g.(145
536610_?)_(?_14574
0218)del
NCBI35 (hg17)NC_000008.9Chr8145,536,610145,740,218

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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