A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590398



Internal ID20963469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50433361..50876126hg38UCSC Ensembl
chr15:50725558..51168323hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38442766
hg19442766
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238103
Samples
Known GenesSPPL2A, TRPM7, USP50, USP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590398
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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