A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083162



Internal ID21439929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3656330..3656330hg38UCSC Ensembl
chr16:3706331..3706331hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661255
Supporting Variants
SamplesHG00732
Known GenesDNASE1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083162
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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