A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561344



Internal ID20934415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184100996..184102016hg38UCSC Ensembl
chr3:183818784..183819804hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381021
hg191021
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260579
Samples
Known GenesHTR3E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561344
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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