A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527114



Internal ID15454407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:72662965..72667549hg38UCSC Ensembl
Innerchr4:73528682..73533266hg19UCSC Ensembl
Innerchr4:73747546..73752130hg18UCSC Ensembl
Innerchr4:73893717..73898301hg17UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg384585
hg194585
hg184585
hg174585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703496
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527114
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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