A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235949



Internal ID20802989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2965689..2967475hg38UCSC Ensembl
chr11:2986919..2988705hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381787
hg191787
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582215
Supporting Variants
Samples
Known GenesNAP1L4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235949
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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