A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13702391



Internal ID21224214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148849006..148849323hg38UCSC Ensembl
chr3:148566793..148567110hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2808438
Supporting Variants
Samples
Known GenesCPB1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13702391
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.984375


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