A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271984



Internal ID20839024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45839665..45854771hg38UCSC Ensembl
chr6:45807402..45822508hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3815107
hg1915107
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556516
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271984
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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