A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592350



Internal ID20965421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50963194..50964202hg38UCSC Ensembl
chr13:51537330..51538338hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg381009
hg191009
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233067
Samples
Known GenesRNASEH2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592350
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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