A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580962



Internal ID16368371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:10011618..10015790hg38UCSC Ensembl
Innerchr2:10151745..10155917hg19UCSC Ensembl
Innerchr2:10069196..10073368hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg384173
hg194173
hg184173
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6691n54
Supporting Variantsnssv903701
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580962
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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