A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498350



Internal ID275341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:106286136..106418495hg38UCSC Ensembl
chr10:108045894..108178253hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38132360
hg19132360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037744
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498350
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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