A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582026



Internal ID20955097
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 StatusM
Merged Variants
Supporting Variantsnssv18229610
Samples
Known GenesHNRNPA1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582026
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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