A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695360



Internal ID15432012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:458317..481679hg38UCSC Ensembl
Innerchr4:452106..475468hg19UCSC Ensembl
Innerchr4:442106..465468hg18UCSC Ensembl
Innerchr4:442106..465468hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3823363
hg1923363
hg1823363
hg1723363
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517948
Supporting Variants
Samples
Known GenesABCA11P, ZNF721
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695360
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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