A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1008n145



Internal ID22814024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8431804..8434846hg38UCSC Ensembl
chr6:8432037..8435079hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg383043
hg193043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117308, nsv3117631, nsv3110643
Samplessample154, sample413, sample420, sample369, sample41, sample347, sample387, sample302, sample331, sample386
Known GenesSLC35B3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1008n145
Frequency
Sample Size467
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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