A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527296



Internal ID15107903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:87811759..87812379hg38UCSC Ensembl
Innerchr4:88732911..88733531hg19UCSC Ensembl
Innerchr4:88951935..88952555hg18UCSC Ensembl
Innerchr4:89090090..89090710hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38621
hg19621
hg18621
hg17621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv322n21
Supporting Variantsnssv703712
Samples
Known GenesIBSP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527296
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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