A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602924



Internal ID16043647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35537534..35782522hg38UCSC Ensembl
Innerchr6:35505311..35750299hg19UCSC Ensembl
Innerchr6:35613289..35858277hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38244989
hg19244989
hg18244989
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1058210
Samples
Known GenesARMC12, CLPSL1, CLPSL2, FKBP5, LOC285847, MIR5690
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602924
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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