A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522372



Internal ID15449665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:81625416..81727591hg38UCSC Ensembl
Innerchr13:82199551..82301726hg19UCSC Ensembl
Innerchr13:81097552..81199727hg18UCSC Ensembl
Innerchr13:81097552..81199727hg17UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38102176
hg19102176
hg18102176
hg17102176
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv115n21
Supporting Variantsnssv695152
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522372
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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