A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569325



Internal ID20942396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168252207..168253211hg38UCSC Ensembl
chr5:167679212..167680216hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381005
hg191005
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267591
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569325
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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