A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547055



Internal ID20920260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:50886997..50898537hg38UCSC Ensembl
chr3:50924428..50935968hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3811541
hg1911541
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260765
Samples
Known GenesDOCK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547055
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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