A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519121



Internal ID15099728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50804835..50829414hg38UCSC Ensembl
Innerchr19:51308092..51332670hg19UCSC Ensembl
Innerchr19:55999904..56024482hg18UCSC Ensembl
Innerchr19:55999904..56024482hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3824580
hg1924579
hg1824579
hg1724579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv203n21
Supporting Variantsnssv696597
Samples
Known GenesKLK1, KLK15, MGC45922
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519121
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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