A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389562



Internal ID21047115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121952801..121957100hg38UCSC Ensembl
chr4:122873956..122878255hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210229
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389562
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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