A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557419



Internal ID20930490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151747453..151748580hg38UCSC Ensembl
chr5:151127014..151128141hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg381128
hg191128
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268721
Samples
Known GenesATOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557419
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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