A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556489



Internal ID20929560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:176514261..176515966hg38UCSC Ensembl
chr3:176232049..176233754hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg381706
hg191706
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263289
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556489
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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