A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497926



Internal ID274940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111082552..111085401hg38UCSC Ensembl
chr10:112842310..112845159hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg382850
hg192850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041101
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497926
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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