A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887882



Internal ID22662880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128440005..128450492hg38UCSC Ensembl
chr3:128158848..128169335hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3810488
hg1910488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391203
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887882
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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