A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv208n54



Internal ID20133632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25303147..25333196hg38UCSC Ensembl
chr1:25629638..25659687hg19UCSC Ensembl
chr1:25502225..25532274hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3830050
hg1930050
hg1830050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545862, nsv545864, nsv545865
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv208n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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