A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394176



Internal ID21051729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103150235..103165704hg38UCSC Ensembl
chr4:104071392..104086861hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3815470
hg1915470
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209453
Samples
Known GenesCENPE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394176
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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