A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592011



Internal ID20965082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66384469..66384715hg38UCSC Ensembl
chr15:66676807..66677053hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38247
hg19247
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238945
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592011
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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