A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576458



Internal ID20949529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24980406..24981563hg38UCSC Ensembl
chr15:25225553..25226710hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381158
hg191158
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239388
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576458
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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