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nsv4203894

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,396

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 45 SVs from 8 studies. See in: genome view    
Remapped(Score: Perfect):118,139,470-118,144,865Question Mark
Overlapping variant regions from other studies: 45 SVs from 8 studies. See in: genome view    
Submitted genomic118,010,185-118,015,580Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4203894RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr11118,139,470118,144,865
nsv4203894Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr11118,010,185118,015,580

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15804980deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15804980RemappedPerfectNC_000011.10:g.118
139470_118144865de
l
GRCh38.p12First PassNC_000011.10Chr11118,139,470118,144,865
nssv15804980Submitted genomicNC_000011.9:g.1180
10185_118015580del
GRCh37.p13NC_000011.9Chr11118,010,185118,015,580

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)
nssv158049804.6e-005121694
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