A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8886n54



Internal ID20142310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1086705..1087362hg38UCSC Ensembl
chr4:1080493..1081150hg19UCSC Ensembl
chr4:1070493..1071150hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38658
hg19658
hg18658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593259, nsv593251, nsv593258, nsv593264, nsv593260, nsv593268
Samples
Known GenesRNF212
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8886n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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