A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5390n100



Internal ID22791477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:131497996..131626271hg38UCSC Ensembl
chr4:132419151..132547426hg19UCSC Ensembl
chr4:132638601..132766876hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38128276
hg19128276
hg18128276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026146, nsv1032908
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)dgv5390n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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