A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502191



Internal ID279064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103310148..103311247hg38UCSC Ensembl
chr10:105069905..105071004hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040014
Samples
Known GenesPCGF6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502191
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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