A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594018



Internal ID20967089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:24595891..24953310hg38UCSC Ensembl
chr13:25170029..25527448hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38357420
hg19357420
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1779n223
Supporting Variantsnssv18222911
Samples
Known GenesATP12A, CENPJ, RNF17, TPTE2P1, TPTE2P6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594018
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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