A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066380



Internal ID21476527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66445172..66445231hg38UCSC Ensembl
chr1:66910855..66910914hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578864
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066380
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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