A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581014



Internal ID16368423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14007193..14072241hg38UCSC Ensembl
Innerchr2:14147318..14212366hg19UCSC Ensembl
Innerchr2:14064769..14129817hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3865049
hg1965049
hg1865049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv903817
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581014
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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