A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238443



Internal ID20805483
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 StatusS
Merged Variantsnsv6586111
Supporting Variants
Samples
Known GenesTARSL2, TM2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238443
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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