A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191460



Internal ID21330319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64553153..64553153hg38UCSC Ensembl
chr11:64320625..64320625hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg383021
hg193021
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3938295
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191460
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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