A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218543



Internal ID20785583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74907421..74911818hg38UCSC Ensembl
chr11:74618466..74622863hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg384398
hg194398
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590804
Supporting Variants
Samples
Known GenesXRRA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218543
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00018


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