A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv369n54



Internal ID20133793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93822968..93825527hg38UCSC Ensembl
chr1:94288524..94291083hg19UCSC Ensembl
chr1:94061112..94063671hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg382560
hg192560
hg182560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv546826, nsv546828, nsv546836, nsv546827
Samples
Known GenesBCAR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv369n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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