A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17147361



Internal ID21495778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109337068..109337068hg38UCSC Ensembl
chr8:110349297..110349297hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5629283
Supporting Variants
SamplesNA19238
Known GenesENY2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17147361
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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