A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5512855



Internal ID289400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:109165093..109287196hg38UCSC Ensembl
chr10:110924851..111046954hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38122104
hg19122104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039639
Samples
Known GenesRNU6-53P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5512855
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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