A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417460



Internal ID21075013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:31164337..31164768hg38UCSC Ensembl
chr9:31164335..31164766hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181715
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417460
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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