A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3946970



Internal ID21367041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3876683..3876683hg38UCSC Ensembl
chr9:3876683..3876683hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204542
SamplesHG002
Known GenesGLIS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3946970
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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