A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094510



Internal ID21505856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62521382..62521382hg38UCSC Ensembl
chr17:60598743..60598743hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381498
hg191498
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652908
Supporting Variants
SamplesNA19983
Known GenesTLK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094510
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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