A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527523



Internal ID15454816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:53877515..53957152hg38UCSC Ensembl
Innerchr13:54451650..54531287hg19UCSC Ensembl
Innerchr13:53349651..53429288hg18UCSC Ensembl
Innerchr13:53349651..53429288hg17UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3879638
hg1979638
hg1879638
hg1779638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703977
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527523
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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