A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3940835



Internal ID21360904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34593236..34593288hg38UCSC Ensembl
chr16:46398167..46398219hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15184235
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3940835
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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