A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233932



Internal ID20800973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63639724..63639891hg38UCSC Ensembl
chr11:63407196..63407363hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582421
Supporting Variants
Samples
Known GenesATL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233932
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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