A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110371



Internal ID21293637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15425603..15427468hg38UCSC Ensembl
Innerchr19:15536414..15538279hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381866
hg191866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101922
Samplessample110
Known GenesWIZ
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110371
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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