A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523344



Internal ID15450637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:33023424..33377121hg38UCSC Ensembl
Innerchr4:33025046..33378743hg19UCSC Ensembl
Innerchr4:32701441..33055138hg18UCSC Ensembl
Innerchr4:32847612..33201309hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38353698
hg19353698
hg18353698
hg17353698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699093
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523344
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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