A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569801



Internal ID20942872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142544020..142544174hg38UCSC Ensembl
chr3:142262862..142263016hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262471
Samples
Known GenesATR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569801
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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