A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580046



Internal ID20953117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35334038..35334803hg38UCSC Ensembl
chr15:35626239..35627004hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38766
hg19766
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237958
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580046
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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