A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433962



Internal ID21395964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184158796..184159580hg38UCSC Ensembl
chr3:183876584..183877368hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv541n172
Supporting Variantsnssv15752929
SamplesNB07
Known GenesDVL3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433962
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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