A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704236



Internal ID15440888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:79859756..79864663hg38UCSC Ensembl
Innerchr5:79155579..79160486hg19UCSC Ensembl
Innerchr5:79191335..79196242hg18UCSC Ensembl
Innerchr5:79191335..79196242hg17UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg384908
hg194908
hg184908
hg174908
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527750
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704236
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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