A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579884



Internal ID20952955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49960034..49961055hg38UCSC Ensembl
chr15:50252231..50253252hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg381022
hg191022
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238074
Samples
Known GenesATP8B4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579884
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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