A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279200



Internal ID20846240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97714491..97714839hg38UCSC Ensembl
chr8:98726719..98727067hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557184
Supporting Variants
Samples
Known GenesMTDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279200
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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