A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090624



Internal ID21267737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:92480024..92485233hg38UCSC Ensembl
Innerchr1:92945581..92950790hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg385210
hg195210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113767
Supporting Variants
Samplessample116
Known GenesGFI1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090624
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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