A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527026



Internal ID15107633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185404275..185632326hg38UCSC Ensembl
Innerchr4:186325429..186553480hg19UCSC Ensembl
Innerchr4:186562423..186790474hg18UCSC Ensembl
Innerchr4:186700578..186928629hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38228052
hg19228052
hg18228052
hg17228052
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703401
Samples
Known GenesC4orf47, CCDC110, PDLIM3, SORBS2, UFSP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527026
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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