A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602705



Internal ID16390114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32625121..32658151hg38UCSC Ensembl
Innerchr6:32592898..32625928hg19UCSC Ensembl
Innerchr6:32700876..32733906hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3833031
hg1933031
hg1833031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10584n54
Supporting Variantsnssv1056504, nssv1056508, nssv1056495, nssv1056498, nssv1056490, nssv1056510, nssv1056506, nssv1056496, nssv1056491, nssv1056502, nssv1056503, nssv1056497, nssv1056493, nssv1056500, nssv1056486, nssv1056509, nssv1056487, nssv1056492, nssv1056488, nssv1056507, nssv1056499, nssv1056505, nssv1056501, nssv1056494, nssv1056489
Samples
Known GenesHLA-DQA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602705
Frequency
Sample Size17421
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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