A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526999



Internal ID15107606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:50866797..50878615hg38UCSC Ensembl
Innerchr13:51440933..51452751hg19UCSC Ensembl
Innerchr13:50338934..50350752hg18UCSC Ensembl
Innerchr13:50338934..50350752hg17UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3811819
hg1911819
hg1811819
hg1711819
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703374
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526999
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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