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nsv5522931

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,785

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 183 SVs from 30 studies. See in: genome view    
Submitted genomic36,500,040-36,509,824Question Mark
Overlapping variant regions from other studies: 183 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):36,990,942-37,000,726Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5522931Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,500,04036,509,824
nsv5522931RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,990,94237,000,726

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723106deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723106Submitted genomicNC_000019.10:g.365
00040_36509824del
GRCh38 (hg38)NC_000019.10Chr1936,500,04036,509,824
nssv17723106RemappedPerfectNC_000019.9:g.3699
0942_37000726del
GRCh37.p13First PassNC_000019.9Chr1936,990,94237,000,726

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)
nssv17723106<0.00126404
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