A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566560



Internal ID20939631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27558530..27563285hg38UCSC Ensembl
chr9:27558528..27563283hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg384756
hg194756
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280420
Samples
Known GenesC9orf72
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566560
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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