A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594776



Internal ID20967847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65229625..65230890hg38UCSC Ensembl
chr15:65521963..65523228hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381266
hg191266
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238879
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594776
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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