A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524556



Internal ID15105163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51062718..51068811hg38UCSC Ensembl
Innerchr19:51565975..51572068hg19UCSC Ensembl
Innerchr19:56257787..56263880hg18UCSC Ensembl
Innerchr19:56257787..56263880hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg386094
hg196094
hg186094
hg176094
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700510
Samples
Known GenesKLK13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524556
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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