A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5384n100



Internal ID22791471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:127473502..127588121hg38UCSC Ensembl
chr4:128394657..128509276hg19UCSC Ensembl
chr4:128614107..128728726hg18UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38114620
hg19114620
hg18114620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017325, nsv1015564
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)dgv5384n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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