A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596942



Internal ID16384351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5511877..5721950hg38UCSC Ensembl
Innerchr5:5511990..5722063hg19UCSC Ensembl
Innerchr5:5564990..5775063hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg38210074
hg19210074
hg18210074
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1023697
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596942
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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