A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573336



Internal ID20946407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140992201..141136815hg38UCSC Ensembl
chr3:140711043..140855657hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38144615
hg19144615
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259762
Samples
Known GenesSPSB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573336
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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