A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090972



Internal ID21463948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65011000..65011000hg38UCSC Ensembl
chr16:65044903..65044903hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662289
Supporting Variants
SamplesHG03065
Known GenesCDH11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090972
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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