A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565709



Internal ID20938780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149652645..149652788hg38UCSC Ensembl
chr3:149370432..149370575hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262589
Samples
Known GenesWWTR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565709
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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