A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065844



Internal ID21502625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45523568..45523722hg38UCSC Ensembl
chr1:45989240..45989394hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584499
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065844
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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