A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv869n54



Internal ID22768764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:238767053..238789322hg38UCSC Ensembl
chr1:238930353..238952622hg19UCSC Ensembl
chr1:236996976..237019245hg18UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3822270
hg1922270
hg1822270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv549427, nsv549428
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv869n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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