A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224417



Internal ID20791457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34037343..34038280hg38UCSC Ensembl
chr11:34058890..34059827hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38938
hg19938
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585385
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224417
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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