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nsv4195214

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 27 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):113,975,724-113,975,794Question Mark
Overlapping variant regions from other studies: 27 SVs from 6 studies. See in: genome view    
Submitted genomic113,846,446-113,846,516Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4195214RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr11113,975,724113,975,794
nsv4195214Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr11113,846,446113,846,516

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15804251deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15804251RemappedPerfectNC_000011.10:g.113
975724_113975794de
l
GRCh38.p12First PassNC_000011.10Chr11113,975,724113,975,794
nssv15804251Submitted genomicNC_000011.9:g.1138
46446_113846516del
GRCh37.p13NC_000011.9Chr11113,846,446113,846,516

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)
nssv158042514.6e-005121694
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