A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596977



Internal ID16384386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7023183..7054854hg38UCSC Ensembl
Innerchr5:7023296..7054967hg19UCSC Ensembl
Innerchr5:7076296..7107967hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3831672
hg1931672
hg1831672
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1023780
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596977
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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