A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085898



Internal ID21410726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2811491..2811491hg38UCSC Ensembl
chr16:2861492..2861492hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655439
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085898
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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