A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670591



Internal ID15060557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:73616..141070hg38UCSC Ensembl
Innerchr4:73508..134851hg19UCSC Ensembl
Innerchr4:63508..124851hg18UCSC Ensembl
Innerchr4:63508..124851hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3867455
hg1961344
hg1861344
hg1761344
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)nssv670591
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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