A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026941



Internal ID19116159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:45935900..46292368hg38UCSC Ensembl
Innerchr8:46847522..47203990hg19UCSC Ensembl
Innerchr8:46966687..47323155hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38356469
hg19356469
hg18356469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7201n100
Supporting Variantsnssv3687378
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)nsv1026941
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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