A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583952



Internal ID16371361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:183631199..183729677hg38UCSC Ensembl
Innerchr2:184495927..184594404hg19UCSC Ensembl
Innerchr2:184204172..184302649hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3898479
hg1998478
hg1898478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv928046
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583952
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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