A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664011



Internal ID15053977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:73616..94493hg38UCSC Ensembl
Innerchr4:73508..94380hg19UCSC Ensembl
Innerchr4:63508..84380hg18UCSC Ensembl
Innerchr4:63508..84380hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3820878
hg1920873
hg1820873
hg1720873
Variant TypeCNV gain
Copy Number
Allele State
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)nssv664011
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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