A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv202n54



Internal ID18992378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25266592..25293098hg38UCSC Ensembl
chr1:25593083..25619589hg19UCSC Ensembl
chr1:25465670..25492176hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3826507
hg1926507
hg1826507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545832, nsv545829
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv202n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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