A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9193n54



Internal ID22777088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106134539..106139684hg38UCSC Ensembl
chr4:107055696..107060841hg19UCSC Ensembl
chr4:107275145..107280290hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg385146
hg195146
hg185146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv595010, nsv595009
Samples
Known GenesTBCK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9193n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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