A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15193152



Internal ID21332039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119253539..119253539hg38UCSC Ensembl
chr11:119124249..119124249hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3931639
Supporting Variants
SamplesHG002
Known GenesCBL
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15193152
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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