A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521458



Internal ID15448751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:84328425..84411938hg38UCSC Ensembl
Innerchr13:84902560..84986073hg19UCSC Ensembl
Innerchr13:83800561..83884074hg18UCSC Ensembl
Innerchr13:83800561..83884074hg17UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3883514
hg1983514
hg1883514
hg1783514
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698068
Samples
Known GenesLINC00333, MIR548F1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521458
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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