A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568575



Internal ID20941646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183859013..183859638hg38UCSC Ensembl
chr3:183576801..183577426hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260566
Samples
Known GenesPARL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568575
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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