A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274792



Internal ID20841832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83497722..83901118hg38UCSC Ensembl
chr6:84207441..84610837hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg38403397
hg19403397
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563283
Supporting Variants
Samples
Known GenesCYB5R4, PRSS35, RIPPLY2, SNAP91
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274792
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00658


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