A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1099n145



Internal ID22814115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17803032..17806058hg38UCSC Ensembl
chr7:17842655..17845681hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg383027
hg193027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3110507, nsv3111914
Samplessample404, sample26
Known GenesSNX13
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1099n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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