A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579144



Internal ID20952215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26250459..26250796hg38UCSC Ensembl
chr15:26495606..26495943hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239408
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579144
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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