A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9457n54



Internal ID22777352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:189108728..190044201hg38UCSC Ensembl
chr4:190029882..190965356hg19UCSC Ensembl
chr4:190266876..191202350hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38935474
hg19935475
hg18935475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596523, nsv596524
Samples
Known GenesFRG1, FRG2, LOC100288255, LOC283788
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9457n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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