A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247757



Internal ID20814797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157093509..157094912hg38UCSC Ensembl
chr1:157063301..157064704hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg381404
hg191404
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538631
Supporting Variants
Samples
Known GenesETV3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247757
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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