A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578799



Internal ID20951870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43017538..43018078hg38UCSC Ensembl
chr15:43309736..43310276hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239548
Samples
Known GenesUBR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578799
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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