A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268535



Internal ID20835575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113617335..113619694hg38UCSC Ensembl
chr6:113938537..113940896hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382360
hg192360
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560512
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268535
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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