A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089749



Internal ID21502871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66701974..66705030hg38UCSC Ensembl
chr16:66735877..66738933hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg383057
hg193057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594813
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089749
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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