A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474142



Internal ID21131695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41756570..41765728hg38UCSC Ensembl
chr12:42150372..42159530hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg389159
hg199159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001122
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474142
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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