A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454359



Internal ID21111912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130553326..130563205hg38UCSC Ensembl
chr9:133428713..133438592hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg389880
hg199880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174697
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454359
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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