A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579074



Internal ID20952145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49891528..49892055hg38UCSC Ensembl
chr15:50183725..50184252hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238073
Samples
Known GenesATP8B4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579074
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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