A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192361



Internal ID21331236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122836537..122836537hg38UCSC Ensembl
chr11:122707245..122707245hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3953840
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192361
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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