A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082624



Internal ID21406950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30187967..30188530hg38UCSC Ensembl
chr16:30199288..30199851hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599067
Supporting Variants
SamplesHG00512
Known GenesCORO1A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082624
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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