A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9363n54



Internal ID22777258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:162347904..162408149hg38UCSC Ensembl
chr4:163269056..163329301hg19UCSC Ensembl
chr4:163488506..163548751hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3860246
hg1960246
hg1860246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596004, nsv595995
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9363n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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