A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091771



Internal ID21489637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:51270634..51270634hg38UCSC Ensembl
chr16:51304545..51304545hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652579
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091771
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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