A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230345



Internal ID20797385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74838886..74839232hg38UCSC Ensembl
chr10:76598644..76598990hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584969
Supporting Variants
Samples
Known GenesKAT6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230345
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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