A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893976



Internal ID18838144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:87973083..87983033hg38UCSC Ensembl
Outerchr4:87973083..87983033hg38UCSC Ensembl
Innerchr4:88894235..88904185hg19UCSC Ensembl
Outerchr4:88894235..88904185hg19UCSC Ensembl
Innerchr4:89113259..89123209hg18UCSC Ensembl
Outerchr4:89113259..89123209hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg389951
hg199951
hg189951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797234
Samples
Known GenesSPP1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893976
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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