A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553941



Internal ID20927051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3324655..3325061hg38UCSC Ensembl
chr3:3366339..3366745hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38407
hg19407
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553941
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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