A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024295



Internal ID18766828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:70319246..70401849hg38UCSC Ensembl
Innerchr8:71231481..71314084hg19UCSC Ensembl
Innerchr8:71394035..71476638hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3882604
hg1982604
hg1882604
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689523
Samples
Known GenesNCOA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024295
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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