A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv989319



Internal ID16283275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:6376326..6391567hg38UCSC Ensembl
Innerchr4:6378053..6393294hg19UCSC Ensembl
Innerchr4:6428954..6444195hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3815242
hg1915242
hg1815242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593499
Supporting Variants
Samples
Known GenesPPP2R2C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv989319
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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