A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv579n145



Internal ID22813595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43775509..43782709hg38UCSC Ensembl
chr19:44279661..44286861hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg387201
hg197201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116859, nsv3114970
Samplessample322, sample321
Known GenesKCNN4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv579n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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