A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259986



Internal ID20827026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37070177..37070574hg38UCSC Ensembl
chr3:37111668..37112065hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554014
Supporting Variants
Samples
Known GenesLRRFIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259986
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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