A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457254



Internal ID21114807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93740301..93748700hg38UCSC Ensembl
chr12:94134077..94142476hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg388400
hg198400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192843
Samples
Known GenesCRADD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457254
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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