A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv993063



Internal ID16287019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:11303486..11326342hg38UCSC Ensembl
Innerchr4:11305110..11327966hg19UCSC Ensembl
Innerchr4:10914208..10937064hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3822857
hg1922857
hg1822857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593736
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv993063
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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