A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116614



Internal ID21504234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52764531..52764531hg38UCSC Ensembl
chr20:51381070..51381070hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667111
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116614
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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