A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581064



Internal ID16021787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:15871387..15901880hg38UCSC Ensembl
Innerchr2:16011511..16042003hg19UCSC Ensembl
Innerchr2:15928962..15959454hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3830494
hg1930493
hg1830493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv903974
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581064
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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