A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114128



Internal ID21297394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35167717..35173998hg38UCSC Ensembl
Innerchr19:35658620..35664901hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg386282
hg196282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv567n145
Supporting Variantsnssv14100339
Samplessample147
Known GenesFXYD5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114128
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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