A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv548n145



Internal ID22813564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9162842..9180468hg38UCSC Ensembl
chr19:9273518..9291144hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3817627
hg1917627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116988, nsv3113150, nsv3111236, nsv3117261
Samplessample70, sample346, sample359, sample423, sample78, sample171, sample369, sample52, sample314, sample358, sample4, sample95, sample143, sample58, sample211, sample310, sample383, sample19, sample44, sample387, sample375, sample157, sample217, sample343, sample299, sample55, sample118, sample79, sample302, sample43, sample295, sample364, sample309, sample27
Known GenesZNF317
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv548n145
Frequency
Sample Size467
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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