A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17119035



Internal ID21458737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31261088..31261088hg38UCSC Ensembl
chr21:32633404..32633404hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668124
Supporting Variants
SamplesHG02587
Known GenesTIAM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17119035
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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