A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv903705



Internal ID15850975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:10447743..10448675hg38UCSC Ensembl
Innerchr2:10587869..10588801hg19UCSC Ensembl
Innerchr2:10505320..10506252hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38933
hg19933
hg18933
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580964
Supporting Variants
Samples
Known GenesODC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv903705
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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