A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8997n54



Internal ID22776892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:34125316..34286927hg38UCSC Ensembl
chr4:34126938..34288549hg19UCSC Ensembl
chr4:33803333..33964944hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38161612
hg19161612
hg18161612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593910, nsv593907, nsv593911
SamplesNINDS_189
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8997n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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