A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457923



Internal ID21115476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64943602..65050844hg38UCSC Ensembl
chr12:65337382..65444624hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg38107243
hg19107243
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186057
Samples
Known GenesFLJ41278, WIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457923
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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