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nsv5483257

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:316,326

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 3948 SVs from 103 studies. See in: genome view    
Submitted genomic11,868,701-12,185,026Question Mark
Overlapping variant regions from other studies: 3952 SVs from 103 studies. See in: genome view    
Remapped(Score: Perfect):11,868,701-12,185,026Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5483257Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr911,868,70112,185,026
nsv5483257RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr911,868,70112,185,026

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17022304deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17022304Submitted genomicNC_000009.12:g.118
68701_12185026del
GRCh38 (hg38)NC_000009.12Chr911,868,70112,185,026
nssv17022304RemappedPerfectNC_000009.11:g.118
68701_12185026del
GRCh37.p13First PassNC_000009.11Chr911,868,70112,185,026

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)
nssv17022304<0.00166404
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