A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271233



Internal ID20838273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34400482..34401586hg38UCSC Ensembl
chr6:34368259..34369363hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381105
hg191105
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557069
Supporting Variants
Samples
Known GenesRPS10-NUDT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271233
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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