A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084909



Internal ID21484754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68124688..68124688hg38UCSC Ensembl
chr17:66120829..66120829hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5659427
Supporting Variants
SamplesNA12329
Known GenesLINC00674
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084909
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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