A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3738459



Internal ID18690054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189636314..189753850hg38UCSC Ensembl
Innerchr3:189354103..189471639hg19UCSC Ensembl
Innerchr3:190836797..190954333hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38117537
hg19117537
hg18117537
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014449
Supporting Variants
Samples
Known GenesTP63
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3738459
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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