A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096988



Internal ID21281918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:105492629..105715939hg38UCSC Ensembl
Innerchr1:106035251..106258561hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38223311
hg19223311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113635
Supporting Variants
Samplessample319
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096988
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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