A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5595n100



Internal ID22791682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:18824078..18949411hg38UCSC Ensembl
chr5:18824187..18949520hg19UCSC Ensembl
chr5:18859944..18985277hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38125334
hg19125334
hg18125334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016689, nsv1027738, nsv1020666
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)dgv5595n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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