A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582340



Internal ID16023063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:80132127..80158023hg38UCSC Ensembl
Innerchr2:80359253..80385149hg19UCSC Ensembl
Innerchr2:80212764..80238660hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3825897
hg1925897
hg1825897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv913799
Samples
Known GenesCTNNA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582340
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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