A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699359



Internal ID15436011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:190385199..190386334hg38UCSC Ensembl
Innerchr3:190102988..190104123hg19UCSC Ensembl
Innerchr3:191585682..191586817hg18UCSC Ensembl
Innerchr3:191585690..191586825hg17UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg381136
hg191136
hg181136
hg171136
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516391
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699359
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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