A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593726



Internal ID20966797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101780868..101920025hg38UCSC Ensembl
chr15:102321071..102460228hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38139158
hg19139158
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238447
Samples
Known GenesOR4F13P, OR4F15, OR4F6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593726
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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