A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190923



Internal ID21329787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68264542..68264542hg38UCSC Ensembl
chr11:68032010..68032010hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951384
Supporting Variants
SamplesHG002
Known GenesC11orf24
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190923
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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