A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602965



Internal ID16390374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:39861447..39891891hg38UCSC Ensembl
Innerchr6:39829223..39859667hg19UCSC Ensembl
Innerchr6:39937201..39967645hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3830445
hg1930445
hg1830445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154310
SamplesHGDP01003
Known GenesDAAM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602965
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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