A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101348



Internal ID21280659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27480183..27882265hg38UCSC Ensembl
Innerchr19:27971091..28373173hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38402083
hg19402083
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110657
Supporting Variants
Samplessample300
Known GenesLINC00662
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101348
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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