A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247096



Internal ID20814136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154613330..154613834hg38UCSC Ensembl
chr1:154585806..154586310hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38505
hg19505
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543122
Supporting Variants
Samples
Known GenesADAR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247096
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00026


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