A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525165



Internal ID15452458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:81625416..81765224hg38UCSC Ensembl
Innerchr13:82199551..82339359hg19UCSC Ensembl
Innerchr13:81097552..81237360hg18UCSC Ensembl
Innerchr13:81097552..81237360hg17UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38139809
hg19139809
hg18139809
hg17139809
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv115n21
Supporting Variantsnssv701239
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525165
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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