A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270056



Internal ID20837096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154517134..154517717hg38UCSC Ensembl
chr6:154838268..154838851hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565146
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270056
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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