A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374219



Internal ID21031772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6941292..6959040hg38UCSC Ensembl
chr4:6943019..6960767hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3817749
hg1917749
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211694
Samples
Known GenesTBC1D14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374219
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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