A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377841



Internal ID21035394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106248301..106264700hg38UCSC Ensembl
chr4:107169458..107185857hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3816400
hg1916400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5397n223
Supporting Variantsnssv18209485
Samples
Known GenesTBCK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377841
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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