A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382170



Internal ID21039723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:128378381..128420638hg38UCSC Ensembl
chr4:129299536..129341793hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3842258
hg1942258
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210303
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382170
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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