A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014449



Internal ID18756983
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 StatusM
Merged Variants
Supporting Variantsnssv3738459
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)nsv1014449
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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