A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190800



Internal ID21329658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13070638..13070638hg38UCSC Ensembl
chr11:13092185..13092185hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3925566
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190800
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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