A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580964



Internal ID16021687
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+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv903705, nssv903704, nssv903706, nssv903707, nssv903703
Samples
Known GenesODC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580964
Frequency
Sample Size17421
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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