A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482078



Internal ID259538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75393172..75395136hg38UCSC Ensembl
chr10:77152930..77154894hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381965
hg191965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038500
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482078
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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