A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17136475



Internal ID21486641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49938672..49938761hg38UCSC Ensembl
chr22:50332320..50332409hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588502
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17136475
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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