A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17115903



Internal ID21463588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23662536..23717852hg38UCSC Ensembl
chr20:23643173..23698489hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3855317
hg1955317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602449
Supporting Variants
SamplesHG03009
Known GenesCST4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17115903
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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