A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500799



Internal ID277725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118346368..118602368hg38UCSC Ensembl
chr10:120105880..120361880hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38256001
hg19256001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040796
Samples
Known GenesLINC00867, PRLHR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500799
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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