A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067373



Internal ID21473013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96992732..96993029hg38UCSC Ensembl
chr1:97458288..97458585hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570310
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067373
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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