A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081883



Internal ID21472058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62838732..62838732hg38UCSC Ensembl
chr15:63130931..63130931hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663830
Supporting Variants
SamplesHG03125
Known GenesTLN2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081883
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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