A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591517



Internal ID21783560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97682242..97682294hg38UCSC Ensembl
chr8:98694470..98694522hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005865
Supporting Variants
Samples
Known GenesMTDH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591517
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer