A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17119365



Internal ID21420897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41806533..41806699hg38UCSC Ensembl
chr21:43226693..43226828hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38167
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597705
Supporting Variants
SamplesHG00731
Known GenesPRDM15
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17119365
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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