A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560597



Internal ID20933668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153881419..153888073hg38UCSC Ensembl
chr3:153599208..153605862hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg386655
hg196655
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560597
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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