A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245389



Internal ID20812429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59346753..59347052hg38UCSC Ensembl
chr18:57013985..57014284hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581761
Supporting Variants
Samples
Known GenesLMAN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245389
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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