A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473151



Internal ID21130704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:47002001..47003100hg38UCSC Ensembl
chr12:47395784..47396883hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000988
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473151
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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