A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432609



Internal ID21090162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:22209101..22442800hg38UCSC Ensembl
chr9:22209100..22442799hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38233700
hg19233700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175838
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432609
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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