A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540330



Internal ID20913620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3841296..3841447hg38UCSC Ensembl
chr3:3882980..3883131hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260018
Samples
Known GenesLRRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540330
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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