A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951742



Internal ID21371812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88295030..88295177hg38UCSC Ensembl
chr16:88328636..88328783hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15175647
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951742
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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