A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568491



Internal ID20941562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134959175..134962349hg38UCSC Ensembl
chr3:134678017..134681191hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg383175
hg193175
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260296
Samples
Known GenesEPHB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568491
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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