A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3946426



Internal ID21366497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2351287..2351287hg38UCSC Ensembl
chr9:2351287..2351287hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204198
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3946426
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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