A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564794



Internal ID20937865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68043591..68044719hg38UCSC Ensembl
chr5:67339419..67340547hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg381129
hg191129
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5783n223
Supporting Variantsnssv18266960
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564794
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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