A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568483



Internal ID20941554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147500370..147501483hg38UCSC Ensembl
chr5:146879933..146881046hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381114
hg191114
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268643
Samples
Known GenesDPYSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568483
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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