A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268826



Internal ID20835866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:36131666..36132880hg38UCSC Ensembl
chr5:36131768..36132982hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg381215
hg191215
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561386
Supporting Variants
Samples
Known GenesLMBRD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268826
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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