A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110628



Internal ID21293894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:37513373..37515797hg38UCSC Ensembl
Innerchr1:37978974..37981398hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382425
hg192425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096630
Samplessample136
Known GenesMEAF6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110628
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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