A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589641



Internal ID20962712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74388201..74394435hg38UCSC Ensembl
chr15:74680541..74686775hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg386235
hg196235
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241932
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589641
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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