A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583277



Internal ID16370686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:146108987..146166665hg38UCSC Ensembl
Innerchr2:146866555..146924233hg19UCSC Ensembl
Innerchr2:146583025..146640703hg18UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3857679
hg1957679
hg1857679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv921226, nssv921225, nssv921224
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583277
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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