A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223206



Internal ID20790246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:21303855..23884356hg38UCSC Ensembl
chr13:21877994..24458495hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg382580502
hg192580502
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585265
Supporting Variants
Samples
Known GenesBASP1P1, FGF9, LINC00327, LINC00424, LINC00539, LINC00540, MICU2, MIPEP, MIPEPP3, SACS, SACS-AS1, SGCG, TNFRSF19, ZDHHC20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223206
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00016


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