A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096835



Internal ID21484307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26557292..26557292hg38UCSC Ensembl
chr16:26568613..26568613hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649043
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096835
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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