A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526256



Internal ID15106863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102791432..102806853hg38UCSC Ensembl
Innerchr4:103712589..103728010hg19UCSC Ensembl
Innerchr4:103931669..103947120hg18UCSC Ensembl
Innerchr4:104069824..104085275hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3815422
hg1915422
hg1815452
hg1715452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702528
Samples
Known GenesUBE2D3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526256
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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