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nsv2817893

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,120

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 872 SVs from 88 studies. See in: genome view    
Submitted genomic6,700,570-6,710,689Question Mark
Overlapping variant regions from other studies: 875 SVs from 88 studies. See in: genome view    
Remapped(Score: Perfect):6,700,570-6,710,689Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv2817893Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr96,700,5706,710,689
nsv2817893RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr96,700,5706,710,689

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv13708951deletionSequencingGenotyping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv13708951Submitted genomicNC_000009.12:g.670
0570_6710689del101
20
GRCh38 (hg38)NC_000009.12Chr96,700,5706,710,689
nssv13708951RemappedPerfectNC_000009.11:g.670
0570_6710689del101
20
GRCh37.p13First PassNC_000009.11Chr96,700,5706,710,689

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv137089510.1561064
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