A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3518126



Internal ID18469721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34919190..34940744hg38UCSC Ensembl
Innerchr11:34940737..34962291hg19UCSC Ensembl
Innerchr11:34897313..34918867hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3821555
hg1921555
hg1821555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055116
Supporting Variants
Samples
Known GenesPDHX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3518126
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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