A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17595914



Internal ID21787957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18032086..18032086hg38UCSC Ensembl
chr11:18053633..18053633hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382159
hg192159
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091175
Supporting Variants
Samples
Known GenesTPH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17595914
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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