A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15193183



Internal ID21332072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134046061..134046061hg38UCSC Ensembl
chr11:133915956..133915956hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3941200
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15193183
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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