A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019368



Internal ID18761902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167180694..167425505hg38UCSC Ensembl
Innerchr6:167594182..167838993hg19UCSC Ensembl
Innerchr6:167514172..167758983hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38244812
hg19244812
hg18244812
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6194n100
Supporting Variantsnssv3655401
Samples
Known GenesTCP10, TCP10L2, TTLL2, UNC93A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019368
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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