A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556378



Internal ID20929449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141771834..141773046hg38UCSC Ensembl
chr3:141490676..141491888hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381213
hg191213
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259782
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556378
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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