A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3941634



Internal ID21361704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88077037..88077037hg38UCSC Ensembl
chr16:88110643..88110643hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15184281
SamplesHG002
Known GenesBANP
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3941634
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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