A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556078



Internal ID20929149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169825087..169826368hg38UCSC Ensembl
chr3:169542875..169544156hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg381282
hg191282
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260465
Samples
Known GenesLRRIQ4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556078
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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