A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581028



Internal ID20954099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52624431..52624748hg38UCSC Ensembl
chr13:53198566..53198883hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232976
Samples
Known GenesHNRNPA1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581028
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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