A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101441



Internal ID21283221
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 StatusS
Merged Variantsnsv3113816
Supporting Variants
Samplessample340
Known GenesSIGLECL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101441
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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