A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132313



Internal ID21511570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35737460..35738225hg38UCSC Ensembl
chr22:36133507..36134272hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38766
hg19766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604096
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132313
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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