A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907142



Internal ID22682347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148335036..148337996hg38UCSC Ensembl
chr3:148052823..148055783hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg382961
hg192961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421357
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907142
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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