A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101495



Internal ID21284454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39538921..39542152hg38UCSC Ensembl
Innerchr19:40029561..40032792hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg383232
hg193232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111493
Supporting Variants
Samplessample361
Known GenesEID2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101495
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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