A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889208



Internal ID22664223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148183016..148183092hg38UCSC Ensembl
chr3:147900803..147900879hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421700
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889208
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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