A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv982991



Internal ID15930261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189647176..189653225hg38UCSC Ensembl
Innerchr3:189364965..189371014hg19UCSC Ensembl
Innerchr3:190847659..190853708hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg386050
hg196050
hg186050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592773
Supporting Variants
Samples
Known GenesTP63
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv982991
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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