A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580967



Internal ID16368376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:10447905..10448777hg38UCSC Ensembl
Innerchr2:10588031..10588903hg19UCSC Ensembl
Innerchr2:10505482..10506354hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38873
hg19873
hg18873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv903715, nssv903714
Samples
Known GenesODC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580967
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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