A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390447



Internal ID21048000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121787768..121794092hg38UCSC Ensembl
chr4:122708923..122715247hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg386325
hg196325
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390447
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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