A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580966



Internal ID16368375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:10447905..10448012hg38UCSC Ensembl
Innerchr2:10588031..10588138hg19UCSC Ensembl
Innerchr2:10505482..10505589hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38108
hg19108
hg18108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv903713
Samples
Known GenesODC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580966
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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