A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577089



Internal ID20950160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92855276..92857749hg38UCSC Ensembl
chr15:93398506..93400979hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382474
hg192474
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239061
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577089
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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