A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096299



Internal ID21430595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28337874..28338329hg38UCSC Ensembl
chr16:28349195..28349650hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590027
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096299
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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