A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090436



Internal ID21413694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58433188..58433188hg38UCSC Ensembl
chr16:58467092..58467092hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651897
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090436
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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