A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595237



Internal ID20968308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32809572..32810384hg38UCSC Ensembl
chr13:33383710..33384522hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228009
Samples
Known GenesLINC00423
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595237
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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