A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602772



Internal ID16390181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32651877..32658151hg38UCSC Ensembl
Innerchr6:32619654..32625928hg19UCSC Ensembl
Innerchr6:32727632..32733906hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg386275
hg196275
hg186275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10597n54
Supporting Variantsnssv1056841, nssv1056848, nssv1056846, nssv1056842, nssv1056847, nssv1056843, nssv1056844, nssv1056845
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602772
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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