A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111778



Internal ID21295044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:112674994..112677496hg38UCSC Ensembl
Innerchr1:113217616..113220118hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg382503
hg192503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108400
Samplessample141
Known GenesMOV10
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111778
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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