A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3631011



Internal ID18582606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:101134867..101529145hg38UCSC Ensembl
Innerchr4:102056024..102450302hg19UCSC Ensembl
Innerchr4:102275047..102669325hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38394279
hg19394279
hg18394279
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011351
Supporting Variants
Samples
Known GenesFLJ20021, MIR8066, PPP3CA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3631011
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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