A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236216



Internal ID20803256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74527351..75035337hg38UCSC Ensembl
chr11:74238396..74746382hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38507987
hg19507987
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590993
Supporting Variants
Samples
Known GenesCHRDL2, MIR4696, NEU3, POLD3, RNF169, SPCS2, XRRA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236216
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00033


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