A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5846n100



Internal ID22791933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179073526..179092186hg38UCSC Ensembl
chr5:178500527..178519187hg19UCSC Ensembl
chr5:178433133..178451793hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3818661
hg1918661
hg1818661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015745, nsv1028000
Samples
Known GenesZNF354C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5846n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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