A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559384



Internal ID20932455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154977556..154980422hg38UCSC Ensembl
chr3:154695345..154698211hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg382867
hg192867
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260380
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559384
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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