A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5446n100



Internal ID22791533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157628595..157640707hg38UCSC Ensembl
chr4:158549747..158561859hg19UCSC Ensembl
chr4:158769197..158781309hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3812113
hg1912113
hg1812113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024128, nsv1025774
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)dgv5446n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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