A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590073



Internal ID20963144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44592518..44593331hg38UCSC Ensembl
chr15:44884716..44885529hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38814
hg19814
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240261
Samples
Known GenesSPG11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590073
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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