A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582354



Internal ID16369763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:82177990..82274929hg38UCSC Ensembl
Innerchr2:82405114..82502053hg19UCSC Ensembl
Innerchr2:82258625..82355564hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3896940
hg1996940
hg1896940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv913817
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582354
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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