A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703739



Internal ID15093705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189255793..189269941hg38UCSC Ensembl
Innerchr4:190176947..190191095hg19UCSC Ensembl
Innerchr4:190413941..190428089hg18UCSC Ensembl
Innerchr4:190552096..190566244hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3814149
hg1914149
hg1814149
hg1714149
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)nssv703739
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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