A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592509



Internal ID20965580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36347330..36348024hg38UCSC Ensembl
chr13:36921467..36922161hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38695
hg19695
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227655
Samples
Known GenesSPG20, SPG20OS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592509
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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