A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv407n206



Internal ID22755711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117821051..117883083hg38UCSC Ensembl
chr5:117156746..117218778hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3862033
hg1962033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5467251, nsv5459753
Samples
Known GenesLOC102467224
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv407n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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