A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694775



Internal ID15084741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4847701..4868790hg38UCSC Ensembl
Innerchr19:4847713..4868802hg19UCSC Ensembl
Innerchr19:4798713..4819802hg18UCSC Ensembl
Innerchr19:4798713..4819802hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3821090
hg1921090
hg1821090
hg1721090
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522005
Supporting Variants
Samples
Known GenesPLIN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694775
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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