A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173546



Internal ID20740586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97663551..97665881hg38UCSC Ensembl
chr8:98675779..98678109hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382331
hg192331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433653
Supporting Variants
Samples
Known GenesMTDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173546
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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