A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271933



Internal ID20838973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134302757..134303395hg38UCSC Ensembl
chr6:134623895..134624533hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566332
Supporting Variants
Samples
Known GenesSGK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271933
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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