A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522763



Internal ID299023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66989156..66994917hg38UCSC Ensembl
chr15:67281494..67287255hg19UCSC Ensembl
Cytoband15q22.32
Allele length
AssemblyAllele length
hg385762
hg195762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704358
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522763
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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