A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17118268



Internal ID21478172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:18365653..18365653hg38UCSC Ensembl
chr21:19737970..19737970hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666179
Supporting Variants
SamplesHG03486
Known GenesTMPRSS15
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17118268
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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