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nsv5514966

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:685

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 183 SVs from 24 studies. See in: genome view    
Submitted genomic46,115,376-46,116,060Question Mark
Overlapping variant regions from other studies: 183 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):43,695,342-43,696,026Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5514966Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1846,115,37646,116,060
nsv5514966RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1843,695,34243,696,026

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17717880deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17717880Submitted genomicNC_000018.10:g.461
15376_46116060del
GRCh38 (hg38)NC_000018.10Chr1846,115,37646,116,060
nssv17717880RemappedPerfectNC_000018.9:g.4369
5342_43696026del
GRCh37.p13First PassNC_000018.9Chr1843,695,34243,696,026

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)
nssv17717880<0.00126402
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