A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv697n145



Internal ID22813713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:19018903..19023283hg38UCSC Ensembl
chr21:20391222..20395602hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg384381
hg194381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113695, nsv3113432, nsv3116379, nsv3117538, nsv3112798, nsv3117566
Samplessample190, sample41, sample213, sample96, sample153, sample393, sample139
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv697n145
Frequency
Sample Size467
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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