A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581065



Internal ID16368474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:16300582..16370115hg38UCSC Ensembl
Innerchr2:16481850..16551383hg19UCSC Ensembl
Innerchr2:16345331..16414864hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3869534
hg1969534
hg1869534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150405
SamplesHGDP01237
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581065
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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