A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581621



Internal ID20954692
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 StatusM
Merged Variants
Supporting Variantsnssv18246938
Samples
Known GenesC18orf32, MIR1539, RPL17-C18orf32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581621
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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