A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700256



Internal ID15436908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3644615..3688474hg38UCSC Ensembl
Innerchr5:3644729..3688588hg19UCSC Ensembl
Innerchr5:3697729..3741588hg18UCSC Ensembl
Innerchr5:3697729..3741588hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3843860
hg1943860
hg1843860
hg1743860
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524348
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700256
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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