A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095820



Internal ID21485123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:139491..139491hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661917
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095820
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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