A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694711



Internal ID15084677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:73616..90996hg38UCSC Ensembl
Innerchr4:73508..90883hg19UCSC Ensembl
Innerchr4:63508..80883hg18UCSC Ensembl
Innerchr4:63508..80883hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3817381
hg1917376
hg1817376
hg1717376
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516451
Supporting Variants
Samples
Known GenesZNF595, ZNF718
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694711
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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