A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192821



Internal ID21331706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112331793..112331793hg38UCSC Ensembl
chr11:112202516..112202516hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3943287
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192821
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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