A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5444n100



Internal ID22791531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156046811..156069699hg38UCSC Ensembl
chr4:156967963..156990851hg19UCSC Ensembl
chr4:157187413..157210301hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3822889
hg1922889
hg1822889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030755, nsv1026377
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)dgv5444n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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