A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525996



Internal ID15453289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:48636666..48648042hg38UCSC Ensembl
Innerchr13:49210802..49222178hg19UCSC Ensembl
Innerchr13:48108803..48120179hg18UCSC Ensembl
Innerchr13:48108803..48120179hg17UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3811377
hg1911377
hg1811377
hg1711377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702221
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525996
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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