A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025174



Internal ID19114392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:137679485..137730515hg38UCSC Ensembl
Innerchr8:138691728..138742758hg19UCSC Ensembl
Innerchr8:138760910..138811940hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3851031
hg1951031
hg1851031
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690053
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)nsv1025174
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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