A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1177n145



Internal ID22814193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39480230..39503164hg38UCSC Ensembl
chr8:39337749..39360683hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3822935
hg1922935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3111691, nsv3110862, nsv3116020, nsv3117105
Samplessample200, sample326, sample21, sample114
Known GenesADAM3A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1177n145
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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