A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262676



Internal ID20829716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46554016..46554596hg38UCSC Ensembl
chr3:46595506..46596086hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542920
Supporting Variants
Samples
Known GenesLRRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262676
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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