A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587824



Internal ID20960895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92824864..92825122hg38UCSC Ensembl
chr15:93368094..93368352hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239057
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587824
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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