A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602383



Internal ID16389792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32510377..32524531hg38UCSC Ensembl
Innerchr6:32478154..32492308hg19UCSC Ensembl
Innerchr6:32586132..32600286hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3814155
hg1914155
hg1814155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1055352, nssv1055358, nssv1055349, nssv1055354, nssv1055346, nssv1055351, nssv1055348, nssv1055353, nssv1055343, nssv1055344, nssv1055357, nssv1055345, nssv1055350, nssv1055355, nssv1055356, nssv1055347
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602383
Frequency
Sample Size17421
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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