A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5396n100



Internal ID20157012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:133889406..134023164hg38UCSC Ensembl
chr4:134810561..134944319hg19UCSC Ensembl
chr4:135030011..135163769hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38133759
hg19133759
hg18133759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028177, nsv1022984, nsv1023994
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5396n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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