A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369809



Internal ID21027362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31642984..31732127hg38UCSC Ensembl
chr4:31644606..31733749hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3889144
hg1989144
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5218n223
Supporting Variantsnssv18214670
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369809
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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