A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704805



Internal ID15441457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:47588423..47659977hg38UCSC Ensembl
Innerchr13:48162558..48234112hg19UCSC Ensembl
Innerchr13:47060559..47132113hg18UCSC Ensembl
Innerchr13:47060559..47132113hg17UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3871555
hg1971555
hg1871555
hg1771555
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528243
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704805
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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