A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225636



Internal ID20792676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25014167..26066860hg38UCSC Ensembl
chr13:25588305..26640998hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381052694
hg191052694
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577502
Supporting Variants
Samples
Known GenesAMER2, ATP8A2, MTMR6, NUPL1, PABPC3, SHISA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225636
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00067


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