A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550474



Internal ID20923615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15533795..15534757hg38UCSC Ensembl
chr3:15575302..15576264hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38963
hg19963
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260391
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550474
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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