A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094130



Internal ID21500970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66380153..66380153hg38UCSC Ensembl
chr16:66414056..66414056hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658365
Supporting Variants
SamplesNA19239
Known GenesCDH5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094130
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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