A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112541



Internal ID21295807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161414072..161421902hg38UCSC Ensembl
Innerchr1:161383862..161391692hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg387831
hg197831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101915
Samplessample38
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112541
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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