A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699453



Internal ID15436105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8930056..8985576hg38UCSC Ensembl
Innerchr19:9040732..9096252hg19UCSC Ensembl
Innerchr19:8901732..8957252hg18UCSC Ensembl
Innerchr19:8901732..8957252hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3855521
hg1955521
hg1855521
hg1755521
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523652
Supporting Variants
Samples
Known GenesMUC16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699453
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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