A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477718



Internal ID21135271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122651168..122659444hg38UCSC Ensembl
chr12:123135715..123143991hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg388277
hg198277
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189458
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477718
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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