A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015626



Internal ID19104843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:106999017..107045157hg38UCSC Ensembl
Innerchr8:108011245..108057385hg19UCSC Ensembl
Innerchr8:108080421..108126561hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3846141
hg1946141
hg1846141
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7280n100
Supporting Variantsnssv3691268
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)nsv1015626
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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