A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117551



Internal ID21448664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60764094..60764094hg38UCSC Ensembl
chr20:59339150..59339150hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669212
Supporting Variants
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117551
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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