A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv658n145



Internal ID22813674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:183035579..183040143hg38UCSC Ensembl
chr2:183900307..183904871hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg384565
hg194565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113874, nsv3113281, nsv3112755
Samplessample349, sample348, sample138
Known GenesNCKAP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv658n145
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer