A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226084



Internal ID20793124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118850501..118851296hg38UCSC Ensembl
chr11:118721210..118722005hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38796
hg19796
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579997
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226084
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00018


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