A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv911190



Internal ID16205146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:57166896..57235505hg38UCSC Ensembl
Innerchr2:57394031..57462640hg19UCSC Ensembl
Innerchr2:57247535..57316144hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3868610
hg1968610
hg1868610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582069
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv911190
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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