A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090114



Internal ID21491672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79004599..79004599hg38UCSC Ensembl
chr17:77000681..77000681hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5647075
Supporting Variants
SamplesNA19238
Known GenesCANT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090114
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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