A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492825



Internal ID270023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97677149..97677220hg38UCSC Ensembl
chr8:98689377..98689448hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17014668
Samples
Known GenesMTDH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492825
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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