A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475686



Internal ID253322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72296923..72299744hg38UCSC Ensembl
chr10:74056681..74059502hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382822
hg192822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475686
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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