A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456446



Internal ID21113999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:22067959..22074186hg38UCSC Ensembl
chr12:22220893..22227120hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg386228
hg196228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456446
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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