A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523089



Internal ID15103696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50817827..50832941hg38UCSC Ensembl
Innerchr19:51321083..51336197hg19UCSC Ensembl
Innerchr19:56012895..56028009hg18UCSC Ensembl
Innerchr19:56012895..56028009hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3815115
hg1915115
hg1815115
hg1715115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv204n21
Supporting Variantsnssv698781
Samples
Known GenesKLK1, KLK15, MGC45922
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523089
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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