A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582767



Internal ID16370176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:117480985..117558733hg38UCSC Ensembl
Innerchr2:118238561..118316309hg19UCSC Ensembl
Innerchr2:117955031..118032779hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3877749
hg1977749
hg1877749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150495
Samples1780862598_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582767
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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