A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028437



Internal ID18770968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:163436396..163494640hg38UCSC Ensembl
Innerchr4:164357548..164415792hg19UCSC Ensembl
Innerchr4:164576998..164635242hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3858245
hg1958245
hg1858245
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3634156
Samples
Known GenesTKTL2, TMA16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028437
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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