A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108196



Internal ID21292313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:89014363..89058546hg38UCSC Ensembl
Innerchr1:89480046..89524229hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3844184
hg1944184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116098
Supporting Variants
Samplessample87
Known GenesGBP1, GBP3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108196
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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