A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521091



Internal ID15101698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9290483..9339353hg38UCSC Ensembl
Innerchr19:9401159..9450029hg19UCSC Ensembl
Innerchr19:9262159..9311029hg18UCSC Ensembl
Innerchr19:9262159..9311029hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3848871
hg1948871
hg1848871
hg1748871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681893, nssv694451, nssv689798
Samples
Known GenesZNF559, ZNF559-ZNF177, ZNF699
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521091
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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