A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936449



Internal ID21356520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32883288..32883288hg38UCSC Ensembl
chr9:32883286..32883286hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204823
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936449
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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