A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477010



Internal ID21134563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37594301..37596700hg38UCSC Ensembl
chr14:38063506..38065905hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193831
Samples
Known GenesFOXA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477010
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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