A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587146



Internal ID20960217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20216092..22917423hg38UCSC Ensembl
chr13:20790231..23491562hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg382701332
hg192701332
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233299
Samples
Known GenesBASP1P1, CRYL1, FGF9, GJB6, IFT88, IL17D, LATS2, LINC00367, LINC00424, LINC00539, LINC00540, MICU2, MIPEPP3, MIR4499, MRP63, N6AMT2, SAP18, SKA3, XPO4, ZDHHC20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587146
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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