A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262576



Internal ID20829616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149036040..149036378hg38UCSC Ensembl
chr3:148753827..148754165hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563400
Supporting Variants
Samples
Known GenesHLTF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262576
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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