A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113976



Internal ID21297242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35169580..35174008hg38UCSC Ensembl
Innerchr19:35660483..35664911hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg384429
hg194429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv568n145
Supporting Variantsnssv14100447, nssv14099008
Samplessample186, sample417
Known GenesFXYD5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113976
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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