A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117595



Internal ID21495944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62160371..62160371hg38UCSC Ensembl
chr20:60735427..60735427hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672342
Supporting Variants
SamplesNA19238
Known GenesSS18L1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117595
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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