A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113816



Internal ID21297082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51256846..51260986hg38UCSC Ensembl
Innerchr19:51760100..51764240hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg384141
hg194141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101441
Samplessample340
Known GenesSIGLECL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113816
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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