A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583250



Internal ID20956321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45345776..45346106hg38UCSC Ensembl
chr13:45919911..45920241hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220680
Samples
Known GenesTPT1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583250
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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