A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384697



Internal ID21042250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112527456..112536934hg38UCSC Ensembl
chr4:113448612..113458090hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg389479
hg199479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384697
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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