A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433874



Internal ID21395876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123478638..123479051hg38UCSC Ensembl
chr3:123197485..123197898hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15754591
SamplesNB07
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433874
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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