A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551761



Internal ID20924894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69075754..69076526hg38UCSC Ensembl
chr3:69124905..69125677hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38773
hg19773
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264022
Samples
Known GenesUBA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551761
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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