A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594331



Internal ID20967402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40662860..40663050hg38UCSC Ensembl
chr15:40955058..40955248hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238266
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594331
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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