A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896214



Internal ID22671303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86263416..86272981hg38UCSC Ensembl
chr3:86312566..86322131hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg389566
hg199566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412694
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896214
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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