A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894633



Internal ID22669707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148143210..148156310hg38UCSC Ensembl
chr3:147860997..147874097hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3813101
hg1913101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427163
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894633
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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