A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017394



Internal ID19106611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25530052..25550174hg38UCSC Ensembl
Innerchr8:25387568..25407690hg19UCSC Ensembl
Innerchr8:25443485..25463607hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3820123
hg1920123
hg1820123
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3760496
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017394
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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