A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590970



Internal ID20964041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89886350..89886816hg38UCSC Ensembl
chr15:90429582..90430048hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240553
Samples
Known GenesAP3S2, C15orf38-AP3S2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590970
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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