A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568359



Internal ID20941430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187132698..187139696hg38UCSC Ensembl
chr3:186850486..186857484hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg386999
hg196999
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261276
Samples
Known GenesRPL39L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568359
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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