A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594519



Internal ID20967590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80482461..80486050hg38UCSC Ensembl
chr15:80774802..80778391hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg383590
hg193590
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239768
Samples
Known GenesARNT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594519
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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