A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088716



Internal ID21433429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24575786..24575786hg38UCSC Ensembl
chr16:24587107..24587107hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663048
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088716
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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