A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114253



Internal ID21297519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35169580..35174589hg38UCSC Ensembl
Innerchr19:35660483..35665492hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg385010
hg195010
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv568n145
Supporting Variantsnssv14100401, nssv14101556, nssv14101109, nssv14101423, nssv14100482, nssv14100452, nssv14101892, nssv14101367, nssv14099672
Samplessample98, sample379, sample42, sample205, sample308, sample169, sample137, sample331, sample188
Known GenesFXYD5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114253
Frequency
Sample Size467
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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