A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217654



Internal ID20784694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66357092..66357440hg38UCSC Ensembl
chr11:66124563..66124911hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585638
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217654
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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