A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699773



Internal ID15436425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:179227433..179286279hg38UCSC Ensembl
Innerchr4:180148587..180207433hg19UCSC Ensembl
Innerchr4:180385581..180444427hg18UCSC Ensembl
Innerchr4:180523736..180582582hg17UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3858847
hg1958847
hg1858847
hg1758847
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523928
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699773
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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