A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492913



Internal ID21150466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28765701..28768900hg38UCSC Ensembl
chr14:29234907..29238106hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180708
Samples
Known GenesFOXG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492913
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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