A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929450



Internal ID21349520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68418418..68418469hg38UCSC Ensembl
chr3:68467568..68467619hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15179760
SamplesHG002
Known GenesFAM19A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929450
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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