A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269768



Internal ID20836808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106672095..106672631hg38UCSC Ensembl
chr6:107119970..107120506hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566724
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269768
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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