A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582228



Internal ID16369637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:76542501..76548257hg38UCSC Ensembl
Innerchr2:76769627..76775383hg19UCSC Ensembl
Innerchr2:76623135..76628891hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg385757
hg195757
hg185757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv912204
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582228
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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