A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192348



Internal ID21331222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121114637..121114637hg38UCSC Ensembl
chr11:120985346..120985346hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3931391
Supporting Variants
SamplesHG002
Known GenesTECTA
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192348
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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