A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473226



Internal ID21130779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:90940516..91014093hg38UCSC Ensembl
chr12:91334293..91407870hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3873578
hg1973578
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187007
Samples
Known GenesCCER1, EPYC, LINC00615
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473226
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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