A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv466n54



Internal ID22768361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106700640..106770988hg38UCSC Ensembl
chr1:107243262..107313610hg19UCSC Ensembl
chr1:107044785..107115133hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3870349
hg1970349
hg1870349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv547328, nsv547327
Samples1782681096_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv466n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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