A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190903



Internal ID21329730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65970847..65970847hg38UCSC Ensembl
chr11:65738318..65738318hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3930249
Supporting Variants
SamplesHG002
Known GenesSART1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190903
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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