A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17111182



Internal ID21487217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:204323790..204323895hg38UCSC Ensembl
chr2:205188513..205188618hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578510
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17111182
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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