A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449388



Internal ID227624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:19410371..19416903hg38UCSC Ensembl
chr4:19411994..19418526hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg386533
hg196533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16946202
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449388
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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