A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524032



Internal ID15451325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25897175..25899165hg38UCSC Ensembl
Innerchr8:25754691..25756681hg19UCSC Ensembl
Innerchr8:25810608..25812598hg18UCSC Ensembl
Innerchr8:25810608..25812598hg17UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg381991
hg191991
hg181991
hg171991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699895
Samples
Known GenesEBF2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524032
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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