A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053344



Internal ID18795875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33007427..33477800hg38UCSC Ensembl
Innerchr11:33028973..33499346hg19UCSC Ensembl
Innerchr11:32985549..33455922hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38470374
hg19470374
hg18470374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1093n100
Supporting Variantsnssv3522348
Samples
Known GenesCSTF3, CSTF3-AS1, DEPDC7, HIPK3, LINC00294, TCP11L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053344
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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