A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv491n145



Internal ID22813507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40816847..40820985hg38UCSC Ensembl
chr17:38973099..38977237hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg384139
hg194139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114227, nsv3113783, nsv3115740, nsv3112780
Samplessample182, sample289, sample349, sample278
Known GenesKRT10, TMEM99
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv491n145
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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