A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581521



Internal ID20954592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94586778..94588424hg38UCSC Ensembl
chr13:95239032..95240678hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381647
hg191647
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236573
Samples
Known GenesTGDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581521
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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