A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190111



Internal ID21328957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94460355..94460355hg38UCSC Ensembl
chr3:94179199..94179199hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3945760
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190111
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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