A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694377



Internal ID15084343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189409239..189415649hg38UCSC Ensembl
Innerchr4:190330393..190336803hg19UCSC Ensembl
Innerchr4:190567387..190573797hg18UCSC Ensembl
Innerchr4:190705542..190711952hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg386411
hg196411
hg186411
hg176411
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517295
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694377
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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