A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450669



Internal ID21108222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128781208..128785362hg38UCSC Ensembl
chr9:131543487..131547641hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg384155
hg194155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176912
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450669
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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