A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477614



Internal ID255188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102094338..102101862hg38UCSC Ensembl
chr10:103854095..103861619hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg387525
hg197525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039891
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477614
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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