A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030608



Internal ID19119827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114830832..114880825hg38UCSC Ensembl
Innerchr8:115843061..115893054hg19UCSC Ensembl
Innerchr8:115912237..115962230hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3849994
hg1949994
hg1849994
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691451
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)nsv1030608
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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