A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192774



Internal ID21331654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87438810..87438810hg38UCSC Ensembl
chr11:87149852..87149852hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3927980
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192774
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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