A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472926



Internal ID21130479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41806154..41814747hg38UCSC Ensembl
chr12:42199956..42208549hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg388594
hg198594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001124
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472926
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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