A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587665



Internal ID20960736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42192968..42194395hg38UCSC Ensembl
chr15:42485166..42486593hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381428
hg191428
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238984
Samples
Known GenesVPS39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587665
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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