A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455337



Internal ID21112890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79891664..79892185hg38UCSC Ensembl
chr9:82506579..82507100hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188677
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455337
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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