A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694508



Internal ID15084474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56080920..56175584hg38UCSC Ensembl
Innerchr19:56592286..56686953hg19UCSC Ensembl
Innerchr19:61284098..61378765hg18UCSC Ensembl
Innerchr19:61284098..61378765hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3894665
hg1994668
hg1894668
hg1794668
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521744
Supporting Variants
Samples
Known GenesZNF444, ZNF787
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694508
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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