A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3942532



Internal ID21362602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189506718..189507582hg38UCSC Ensembl
chr3:189224507..189225371hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38865
hg19865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15180473
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3942532
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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