A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467404



Internal ID21124957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:78352859..78353933hg38UCSC Ensembl
chr12:78746639..78747713hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg381075
hg191075
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191087
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467404
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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