A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110796



Internal ID21294062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151105906..151108734hg38UCSC Ensembl
Innerchr3:150823693..150826521hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg382829
hg192829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105374, nssv14108626, nssv14103537, nssv14106427
Samplessample146, sample369, sample31, sample110
Known GenesMED12L
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110796
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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