A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544908



Internal ID20918146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21858218..21866893hg38UCSC Ensembl
chr3:21899710..21908385hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg388676
hg198676
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261943
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544908
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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