A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568276



Internal ID20941347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6606588..6607311hg38UCSC Ensembl
chr5:6606701..6607424hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5629n223
Supporting Variantsnssv18266938
Samples
Known GenesNSUN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568276
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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