A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100253



Internal ID21286181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:26625984..26629667hg38UCSC Ensembl
Innerchr1:26952475..26956158hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383684
hg193684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117596
Supporting Variants
Samplessample384
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100253
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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