A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110973



Internal ID21294239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:49265193..49281962hg38UCSC Ensembl
Innerchr1:49730865..49747634hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3816770
hg1916770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087712
Samplessample167
Known GenesAGBL4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110973
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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