A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv408n206



Internal ID22755712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:120885498..121207193hg38UCSC Ensembl
chr5:120221193..120542888hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38321696
hg19321696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5469658, nsv5469635
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv408n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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