A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569581



Internal ID20942652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:121192997..121858688hg38UCSC Ensembl
chr3:120911844..121577535hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38665692
hg19665692
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261783
Samples
Known GenesARGFX, EAF2, FBXO40, GOLGB1, HCLS1, IQCB1, POLQ, STXBP5L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569581
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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