A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597635



Internal ID16385044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25959921..26033842hg38UCSC Ensembl
Innerchr5:25960030..26033951hg19UCSC Ensembl
Innerchr5:25995787..26069708hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3873922
hg1973922
hg1873922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9690n54
Supporting Variantsnssv1028054
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597635
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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