A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv903718



Internal ID16197674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:11035269..11086381hg38UCSC Ensembl
Innerchr2:11175395..11226507hg19UCSC Ensembl
Innerchr2:11092846..11143958hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3851113
hg1951113
hg1851113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580971
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)nssv903718
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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