A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481236



Internal ID258724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86111879..86115777hg38UCSC Ensembl
chr10:87871636..87875534hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg383899
hg193899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038305
Samples
Known GenesGRID1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481236
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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