A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1173n145



Internal ID22814189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39375671..39465829hg38UCSC Ensembl
chr8:39233190..39323348hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3890159
hg1990159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3110925, nsv3113994
Samplessample374, sample79
Known GenesADAM3A, ADAM5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1173n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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