A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5483n100



Internal ID22791570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:177824913..177953102hg38UCSC Ensembl
chr4:178746067..178874256hg19UCSC Ensembl
chr4:178983061..179111250hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38128190
hg19128190
hg18128190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022327, nsv1028173
Samples
Known GenesLINC01098, LINC01099
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5483n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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