A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3954857



Internal ID21374926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194268243..194268321hg38UCSC Ensembl
chr3:193986032..193986110hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15179287
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3954857
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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