A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524532



Internal ID15451825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:102698214..102700410hg38UCSC Ensembl
Innerchr13:103350564..103352760hg19UCSC Ensembl
Innerchr13:102148565..102150761hg18UCSC Ensembl
Innerchr13:102148565..102150761hg17UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg382197
hg192197
hg182197
hg172197
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700482
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524532
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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