A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564880



Internal ID20937951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170185275..170186932hg38UCSC Ensembl
chr3:169903063..169904720hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg381658
hg191658
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260490
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564880
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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