A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15204271



Internal ID21343073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86611736..86611736hg38UCSC Ensembl
chr9:89226651..89226651hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3926582
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15204271
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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