A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17118972



Internal ID21458697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:719582..720746hg38UCSC Ensembl
chr20:700226..701390hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381165
hg191165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600884
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17118972
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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