A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567547



Internal ID20940618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164528661..164529963hg38UCSC Ensembl
chr5:163955667..163956969hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381303
hg191303
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268090
Samples
Known GenesLOC102546299
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567547
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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