A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907062



Internal ID22682267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150605456..150605547hg38UCSC Ensembl
chr3:150323243..150323334hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417651
Samples
Known GenesSELT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907062
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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