A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389454



Internal ID21047007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62348201..62400400hg38UCSC Ensembl
chr4:63213919..63266118hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3852200
hg1952200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389454
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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