A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8875n54



Internal ID22776770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:354378..440290hg38UCSC Ensembl
chr4:348167..434079hg19UCSC Ensembl
chr4:338167..424079hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3885913
hg1985913
hg1885913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593201, nsv593200
Samples
Known GenesABCA11P, ZNF141, ZNF721
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8875n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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