A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024931



Internal ID19114149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:43552719..43968893hg38UCSC Ensembl
Innerchr8:43407862..43824036hg19UCSC Ensembl
Innerchr8:43527019..43943193hg18UCSC Ensembl
Cytoband8p11.1
Allele length
AssemblyAllele length
hg38416175
hg19416175
hg18416175
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7189n100
Supporting Variantsnssv3687291, nssv3687289, nssv3687294, nssv3687290, nssv3687292, nssv3687293
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)nsv1024931
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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