A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229610



Internal ID20796650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52601053..52645321hg38UCSC Ensembl
chr13:53175188..53219456hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3844269
hg1944269
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582026
Supporting Variants
Samples
Known GenesHNRNPA1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229610
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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