A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190941



Internal ID21329801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78879317..78879317hg38UCSC Ensembl
chr11:78590362..78590362hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3946849
Supporting Variants
SamplesHG002
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190941
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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