A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381484



Internal ID21039037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:128667385..128677461hg38UCSC Ensembl
chr4:129588540..129598616hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3810077
hg1910077
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210305
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381484
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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