A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190804



Internal ID21329662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14478464..14478464hg38UCSC Ensembl
chr11:14500010..14500010hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3934681
Supporting Variants
SamplesHG002
Known GenesCOPB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190804
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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