A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449744



Internal ID227972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16370006..16405181hg38UCSC Ensembl
chr4:16371629..16406804hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3835176
hg1935176
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16945538
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449744
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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