A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031156



Internal ID19120377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114539278..114608617hg38UCSC Ensembl
Innerchr8:115551507..115620846hg19UCSC Ensembl
Innerchr8:115620683..115690022hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3869340
hg1969340
hg1869340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7291n100
Supporting Variantsnssv3691322
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)nsv1031156
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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