A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490687



Internal ID267938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:952208..979815hg38UCSC Ensembl
chr10:998148..1025755hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3827608
hg1927608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030898
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490687
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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