A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525468



Internal ID301627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45548291..45567209hg38UCSC Ensembl
chr20:44176930..44195848hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3818919
hg1918919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732621
Samples
Known GenesWFDC8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525468
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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