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nsv5508746

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:30,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 226 SVs from 45 studies. See in: genome view    
Submitted genomic2,346,000-2,376,000Question Mark
Overlapping variant regions from other studies: 226 SVs from 45 studies. See in: genome view    
Remapped(Score: Perfect):2,367,230-2,397,230Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5508746Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr112,346,0002,376,000
nsv5508746RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr112,367,2302,397,230

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17043606duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17043606Submitted genomicNC_000011.10:g.234
6000_2376000dup
GRCh38 (hg38)NC_000011.10Chr112,346,0002,376,000
nssv17043606RemappedPerfectNC_000011.9:g.2367
230_2397230dup
GRCh37.p13First PassNC_000011.9Chr112,367,2302,397,230

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)
nssv17043606<0.00126402
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