A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085157



Internal ID21480198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15808726..15808726hg38UCSC Ensembl
chr17:15712040..15712040hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg384964
hg194964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651962
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085157
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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