A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224881



Internal ID20791921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63645037..63645884hg38UCSC Ensembl
chr11:63412509..63413356hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38848
hg19848
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581955
Supporting Variants
Samples
Known GenesATL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224881
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00026


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