A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232034



Internal ID20799074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45645699..45651437hg38UCSC Ensembl
chr11:45667249..45672987hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg385739
hg195739
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587373
Supporting Variants
Samples
Known GenesCHST1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232034
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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