A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv768n54



Internal ID22768663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:199049014..199133482hg38UCSC Ensembl
chr1:199018143..199102610hg19UCSC Ensembl
chr1:197284766..197369233hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3884469
hg1984468
hg1884468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv548936, nsv548931, nsv548934, nsv548933, nsv548932, nsv548939, nsv548935
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv768n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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