A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459242



Internal ID21116795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93050862..93059269hg38UCSC Ensembl
chr12:93444638..93453045hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg388408
hg198408
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190214
Samples
Known GenesLOC643339
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459242
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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