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nsv2801518

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,557

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 296 SVs from 60 studies. See in: genome view    
Submitted genomic207,538,518-207,557,074Question Mark
Overlapping variant regions from other studies: 302 SVs from 60 studies. See in: genome view    
Remapped(Score: Perfect):207,711,863-207,730,419Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv2801518Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1207,538,518207,557,074
nsv2801518RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1207,711,863207,730,419

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv13691375deletionSequencingGenotyping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv13691375Submitted genomicNC_000001.11:g.207
538518_207557074de
l18557
GRCh38 (hg38)NC_000001.11Chr1207,538,518207,557,074
nssv13691375RemappedPerfectNC_000001.10:g.207
711863_207730419de
l18557
GRCh37.p13First PassNC_000001.10Chr1207,711,863207,730,419

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)
nssv1369137516464
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