A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218355



Internal ID20785395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61423000..61423322hg38UCSC Ensembl
chr11:61190472..61190794hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586885
Supporting Variants
Samples
Known GenesCPSF7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218355
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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