A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv207n54



Internal ID20133631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25298555..25320442hg38UCSC Ensembl
chr1:25625046..25646933hg19UCSC Ensembl
chr1:25497633..25519520hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3821888
hg1921888
hg1821888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545860, nsv545859
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv207n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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