A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937295



Internal ID21357364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24479267..24479355hg38UCSC Ensembl
chr16:24490588..24490676hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15184019
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937295
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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