A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581046



Internal ID16368455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14565266..14625076hg38UCSC Ensembl
Innerchr2:14705390..14765200hg19UCSC Ensembl
Innerchr2:14622841..14682651hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3859811
hg1959811
hg1859811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6703n54
Supporting Variantsnssv1150404
SamplesHGDP00630
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581046
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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