A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568820



Internal ID20941891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113729569..113730112hg38UCSC Ensembl
chr3:113448416..113448959hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38544
hg19544
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259246
Samples
Known GenesNAA50
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568820
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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