A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025672



Internal ID18768204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:22868571..23130480hg38UCSC Ensembl
Innerchr8:22726084..22987993hg19UCSC Ensembl
Innerchr8:22782029..23043938hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38261910
hg19261910
hg18261910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3760482
Samples
Known GenesLOC254896, LOC286059, PEBP4, RHOBTB2, TNFRSF10B, TNFRSF10C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025672
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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