A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592568



Internal ID20965639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32463536..32465105hg38UCSC Ensembl
chr13:33037673..33039242hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg381570
hg191570
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237033
Samples
Known GenesN4BP2L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592568
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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