A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582039



Internal ID20955110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48063599..48074744hg38UCSC Ensembl
chr15:48355796..48366941hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3811146
hg1911146
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582039
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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