A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569131



Internal ID20942202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169621652..169622173hg38UCSC Ensembl
chr3:169339440..169339961hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260456
Samples
Known GenesMECOM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569131
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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