A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594132



Internal ID21786175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3870805..3870805hg38UCSC Ensembl
chr11:3892035..3892035hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087310
Supporting Variants
Samples
Known GenesSTIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594132
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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