A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351814



Internal ID21009367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:22196801..22198100hg38UCSC Ensembl
chr2:22419673..22420972hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086310
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351814
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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