A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111840



Internal ID21295106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:227905488..227923164hg38UCSC Ensembl
Innerchr1:228093189..228110865hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3817677
hg1917677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090680
Samplessample116
Known GenesWNT9A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111840
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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