A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15753675



Internal ID21390813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184158796..184159604hg38UCSC Ensembl
chr3:183876584..183877392hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38809
hg19809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433963
Supporting Variants
SamplesNB11
Known GenesDVL3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15753675
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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