A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563245



Internal ID20936316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160421067..160421474hg38UCSC Ensembl
chr3:160138855..160139262hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259836
Samples
Known GenesSMC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563245
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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