A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483788



Internal ID21141341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45888701..46309200hg38UCSC Ensembl
chr14:46357904..46778403hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38420500
hg19420500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188825
Samples
Known GenesLINC00871
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483788
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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