A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082726



Internal ID21498738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70210520..70210520hg38UCSC Ensembl
chr17:68206661..68206661hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5657444
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082726
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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