A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117017



Internal ID21446922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56672750..56679541hg38UCSC Ensembl
chr20:55247806..55254597hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg386792
hg196792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591456
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117017
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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