A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101275



Internal ID21278877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33288601..33289889hg38UCSC Ensembl
Innerchr19:33779507..33780795hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381289
hg191289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113051
Supporting Variants
Samplessample275
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101275
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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