A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1176n145



Internal ID22814192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39478017..39528445hg38UCSC Ensembl
chr8:39335536..39385964hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3850429
hg1950429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113556, nsv3116390, nsv3116846, nsv3115960
Samplessample165, sample374, sample393, sample79
Known GenesADAM3A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1176n145
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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