A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486429



Internal ID263795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52741366..52742978hg38UCSC Ensembl
chr10:54501126..54502738hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg381613
hg191613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035727
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486429
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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