A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115128



Internal ID21298394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:11902434..11917018hg38UCSC Ensembl
Innerchr1:11962491..11977075hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3814585
hg1914585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086317
Samplessample162
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115128
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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