A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9194n54



Internal ID20142618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106134539..106141514hg38UCSC Ensembl
chr4:107055696..107062671hg19UCSC Ensembl
chr4:107275145..107282120hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg386976
hg196976
hg186976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv595012, nsv595011
Samples
Known GenesTBCK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9194n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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