A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022071



Internal ID19111289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:175919582..176011481hg38UCSC Ensembl
Innerchr5:175346585..175438484hg19UCSC Ensembl
Innerchr5:175279191..175371090hg18UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3891900
hg1991900
hg1891900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3649145
Samples
Known GenesTHOC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022071
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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