A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271352



Internal ID20838392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43537855..43538299hg38UCSC Ensembl
chr6:43505592..43506036hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559036
Supporting Variants
Samples
Known GenesXPO5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271352
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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