A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523652



Internal ID15450945
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699453
Samples
Known GenesMUC16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523652
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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