A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698937



Internal ID15435589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167936311..167949886hg38UCSC Ensembl
Innerchr4:168857462..168871037hg19UCSC Ensembl
Innerchr4:169094037..169107612hg18UCSC Ensembl
Innerchr4:169232192..169245767hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3813576
hg1913576
hg1813576
hg1713576
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515790
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698937
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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