A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063406



Internal ID21488557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221498888..221501376hg38UCSC Ensembl
chr1:221672230..221674718hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg382489
hg192489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5573368
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063406
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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