A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545314



Internal ID20918544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13678930..13683198hg38UCSC Ensembl
chr3:13720429..13724697hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg384269
hg194269
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259683
Samples
Known GenesLINC00620
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545314
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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