A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111702



Internal ID21294968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7902672..7918162hg38UCSC Ensembl
Innerchr19:7967557..7983047hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3815491
hg1915491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099613
Samplessample116
Known GenesMAP2K7, TGFBR3L
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111702
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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