A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv968n145



Internal ID22813984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:19072487..19451119hg38UCSC Ensembl
chr5:19072596..19451228hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38378633
hg19378633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116932, nsv3115193
Samplessample274, sample283
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv968n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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