A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483998



Internal ID261421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105982101..105982167hg38UCSC Ensembl
chr7:105622547..105622613hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17001599
Samples
Known GenesCDHR3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483998
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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