A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563286



Internal ID20936357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148103705..148104027hg38UCSC Ensembl
chr3:147821492..147821814hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262559
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563286
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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