A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032991



Internal ID18775525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:106744433..106806807hg38UCSC Ensembl
Innerchr8:107756661..107819035hg19UCSC Ensembl
Innerchr8:107825837..107888211hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3862375
hg1962375
hg1862375
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757333
Samples
Known GenesABRA, OXR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032991
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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