A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571884



Internal ID20944955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145624801..145624855hg38UCSC Ensembl
chr3:145342588..145342642hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571884
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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