A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5219n100



Internal ID22791306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:59397311..59454303hg38UCSC Ensembl
chr4:60263029..60320021hg19UCSC Ensembl
chr4:59945624..60002616hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3856993
hg1956993
hg1856993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009160, nsv1006397
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)dgv5219n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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