A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17118028



Internal ID21496014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63546466..63546466hg38UCSC Ensembl
chr20:62177819..62177819hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668665
Supporting Variants
SamplesNA19238
Known GenesSRMS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17118028
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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