A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487437



Internal ID264776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75243073..75246236hg38UCSC Ensembl
chr10:77002831..77005994hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg383164
hg193164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487437
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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