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nsv6144733

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,703

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 323 SVs from 55 studies. See in: genome view    
Submitted genomic63,897,582-63,912,284Question Mark
Overlapping variant regions from other studies: 323 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):61,974,942-61,989,644Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6144733Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1763,897,58263,912,284
nsv6144733RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1761,974,94261,989,644

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714037deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714037Submitted genomicNC_000017.11:g.638
97582_63912284del
GRCh38 (hg38)NC_000017.11Chr1763,897,58263,912,284
nssv17714037RemappedPerfectNC_000017.10:g.619
74942_61989644del
GRCh37.p13First PassNC_000017.10Chr1761,974,94261,989,644

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)
nssv17714037<0.00146404
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