A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526093



Internal ID15106700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:221560900..221563151hg38UCSC Ensembl
Innerchr2:222425620..222427871hg19UCSC Ensembl
Innerchr2:222133864..222136115hg18UCSC Ensembl
Innerchr2:222251125..222253376hg17UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg382252
hg192252
hg182252
hg172252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702340
Samples
Known GenesEPHA4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526093
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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