A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700602



Internal ID15090568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50817827..50829414hg38UCSC Ensembl
Innerchr19:51321083..51332670hg19UCSC Ensembl
Innerchr19:56012895..56024482hg18UCSC Ensembl
Innerchr19:56012895..56024482hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3811588
hg1911588
hg1811588
hg1711588
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524637
Supporting Variants
Samples
Known GenesKLK1, KLK15, MGC45922
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700602
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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