A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015747



Internal ID19104965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:92409568..92425602hg38UCSC Ensembl
Innerchr8:93421796..93437830hg19UCSC Ensembl
Innerchr8:93490972..93507006hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3816035
hg1916035
hg1816035
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689720
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)nsv1015747
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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