A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv913802



Internal ID16207758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:81960228..82072821hg38UCSC Ensembl
Innerchr2:82187352..82299945hg19UCSC Ensembl
Innerchr2:82040863..82153456hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38112594
hg19112594
hg18112594
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582345
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)nssv913802
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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