A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589999



Internal ID20963070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31240486..31241022hg38UCSC Ensembl
chr15:31532689..31533225hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589999
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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