A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034456



Internal ID18776990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:69974082..70077065hg38UCSC Ensembl
Innerchr8:70886317..70989300hg19UCSC Ensembl
Innerchr8:71048871..71151854hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38102984
hg19102984
hg18102984
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757286
Samples
Known GenesPRDM14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034456
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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