A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897912



Internal ID22673022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16743240..16755782hg38UCSC Ensembl
chr3:16784747..16797289hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3812543
hg1912543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424813
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897912
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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