A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586111



Internal ID20959182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101562826..101789070hg38UCSC Ensembl
chr15:102103029..102329273hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38226245
hg19226245
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238443
Samples
Known GenesTARSL2, TM2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586111
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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