A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3925054



Internal ID21345123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16624276..16624330hg38UCSC Ensembl
chr5:16624385..16624439hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15195834
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3925054
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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