A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190799



Internal ID21329657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13016508..13016508hg38UCSC Ensembl
chr11:13038055..13038055hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3943759
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190799
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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