A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270026



Internal ID20837066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153014566..153015667hg38UCSC Ensembl
chr6:153335701..153336802hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg381102
hg191102
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570279
Supporting Variants
Samples
Known GenesRGS17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270026
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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