A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271306



Internal ID20838346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42601410..42601905hg38UCSC Ensembl
chr6:42569148..42569643hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561722
Supporting Variants
Samples
Known GenesUBR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271306
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00035


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