A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095800



Internal ID21504840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:5278990..5278990hg38UCSC Ensembl
chr16:5328991..5328991hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381050
hg191050
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660003
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095800
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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