A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661845



Internal ID21610150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59959024..59959024hg38UCSC Ensembl
chr17:58036385..58036385hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094663
SamplesNA20509
Known GenesRNFT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661845
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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