A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv206n54



Internal ID18992382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25284602..25316105hg38UCSC Ensembl
chr1:25611093..25642596hg19UCSC Ensembl
chr1:25483680..25515183hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3831504
hg1931504
hg1831504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545853, nsv545854
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv206n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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