A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110174



Internal ID21293440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:222612863..222620817hg38UCSC Ensembl
Innerchr1:222786205..222794159hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg387955
hg197955
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101479
Samplessample397
Known GenesMIA3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110174
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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