A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254559



Internal ID20821599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:149761568..149762226hg38UCSC Ensembl
chr2:150618082..150618740hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541950
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254559
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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