A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470234



Internal ID21127787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:79972897..79997481hg38UCSC Ensembl
chr12:80366677..80391261hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3824585
hg1924585
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178167
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470234
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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