A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270100



Internal ID20837140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155266617..155267221hg38UCSC Ensembl
chr6:155587751..155588355hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564973
Supporting Variants
Samples
Known GenesCLDN20, TFB1M
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270100
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00027


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