A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1003579



Internal ID15950849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:101039155..101039652hg38UCSC Ensembl
Innerchr4:101960312..101960809hg19UCSC Ensembl
Innerchr4:102179335..102179832hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38498
hg19498
hg18498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594950
Supporting Variants
Samples
Known GenesPPP3CA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1003579
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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