A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518154



Internal ID15445447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:71819612..71990617hg38UCSC Ensembl
Innerchr4:72685329..72856334hg19UCSC Ensembl
Innerchr4:72904193..73075198hg18UCSC Ensembl
Innerchr4:73050364..73221369hg17UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38171006
hg19171006
hg18171006
hg17171006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694206
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518154
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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