A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278692



Internal ID20845732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73947725..73947956hg38UCSC Ensembl
chr8:74859960..74860191hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559583
Supporting Variants
Samples
Known GenesTCEB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278692
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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