A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589188



Internal ID20962259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72576474..72577037hg38UCSC Ensembl
chr15:72868815..72869378hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241895
Samples
Known GenesARIH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589188
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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