A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116210



Internal ID21405617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37487445..37488390hg38UCSC Ensembl
chr20:36115847..36116792hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38946
hg19946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592202
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116210
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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