A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695489



Internal ID15432141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19581770..19604985hg38UCSC Ensembl
Innerchr19:19692579..19715794hg19UCSC Ensembl
Innerchr19:19553579..19576794hg18UCSC Ensembl
Innerchr19:19553579..19576794hg17UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3823216
hg1923216
hg1823216
hg1723216
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518076
Supporting Variants
Samples
Known GenesPBX4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695489
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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