A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579014



Internal ID20952085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50062124..50065040hg38UCSC Ensembl
chr15:50354321..50357237hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg382917
hg192917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238075
Samples
Known GenesATP8B4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579014
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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