A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591431



Internal ID20964502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98805765..98806923hg38UCSC Ensembl
chr13:99458019..99459177hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg381159
hg191159
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233392
Samples
Known GenesDOCK9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591431
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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