A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694328



Internal ID15430980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:155516931..155551614hg38UCSC Ensembl
Innerchr4:156438083..156472766hg19UCSC Ensembl
Innerchr4:156657533..156692216hg18UCSC Ensembl
Innerchr4:156795688..156830371hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3834684
hg1934684
hg1834684
hg1734684
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519421
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694328
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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