A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110880



Internal ID21294146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39417204..39528445hg38UCSC Ensembl
Innerchr8:39274723..39385964hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38111242
hg19111242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1174n145
Supporting Variantsnssv14087338, nssv14085832
Samplessample306, sample29
Known GenesADAM3A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110880
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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