A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564044



Internal ID20937115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140469990..140747260hg38UCSC Ensembl
chr3:140188832..140466102hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38277271
hg19277271
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259758
Samples
Known GenesCLSTN2, CLSTN2-AS1, TRIM42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564044
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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