A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv982993



Internal ID15930263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189647635..189649860hg38UCSC Ensembl
Innerchr3:189365424..189367649hg19UCSC Ensembl
Innerchr3:190848118..190850343hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg382226
hg192226
hg182226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592774
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)nssv982993
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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