A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950861



Internal ID21370930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4735334..4735334hg38UCSC Ensembl
chr9:4735334..4735334hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204546
SamplesHG002
Known GenesAK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950861
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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