A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602956



Internal ID16390365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:37941308..38018713hg38UCSC Ensembl
Innerchr6:37909084..37986489hg19UCSC Ensembl
Innerchr6:38017062..38094467hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3877406
hg1977406
hg1877406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1058389
Samples
Known GenesZFAND3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602956
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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