A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246938



Internal ID20813979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:49483986..49487992hg38UCSC Ensembl
chr18:47010356..47014362hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg384007
hg194007
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581621
Supporting Variants
Samples
Known GenesC18orf32, MIR1539, RPL17-C18orf32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246938
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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