A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116904



Internal ID21510827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4227652..4227703hg38UCSC Ensembl
chr20:4208299..4208350hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585798
Supporting Variants
SamplesNA24385
Known GenesADRA1D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116904
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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