A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569557



Internal ID20942628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160572320..160572725hg38UCSC Ensembl
chr3:160290108..160290513hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261056
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569557
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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