A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560671



Internal ID20933742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152623175..152623472hg38UCSC Ensembl
chr5:152002735..152003032hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268731
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560671
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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