A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601508



Internal ID16388917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31269982..31270712hg38UCSC Ensembl
Innerchr6:31237759..31238489hg19UCSC Ensembl
Innerchr6:31345738..31346468hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38731
hg19731
hg18731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10376n54
Supporting Variantsnssv1052370, nssv1052355, nssv1052359, nssv1052375, nssv1052365, nssv1052364, nssv1052376, nssv1052358, nssv1052367, nssv1052366, nssv1052354, nssv1052374, nssv1052371, nssv1052373, nssv1052368, nssv1052362, nssv1052353, nssv1052356, nssv1052361, nssv1052372, nssv1052360, nssv1052357, nssv1052352, nssv1052377, nssv1052369, nssv1052363
Samples
Known GenesHLA-C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601508
Frequency
Sample Size17421
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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