A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421862



Internal ID21079415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21118953..21124872hg38UCSC Ensembl
chr9:21118952..21124871hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg385920
hg195920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176467
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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