A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475876



Internal ID253508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97682241..97682298hg38UCSC Ensembl
chr8:98694469..98694526hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17014669
Samples
Known GenesMTDH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475876
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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