A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550795



Internal ID20923935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49308962..49309729hg38UCSC Ensembl
chr3:49346395..49347162hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262814
Samples
Known GenesUSP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550795
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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