A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17115884



Internal ID21459768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18997495..18998222hg38UCSC Ensembl
chr20:18978139..18978866hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38728
hg19728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594383
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17115884
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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