A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461159



Internal ID21118712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46757801..46761900hg38UCSC Ensembl
chr12:47151584..47155683hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179488
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461159
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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