A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585119



Internal ID20958190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69543250..69548499hg38UCSC Ensembl
chr15:69835589..69840838hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg385250
hg195250
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585119
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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