A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv200n54



Internal ID20133624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25262655..25300841hg38UCSC Ensembl
chr1:25589146..25627332hg19UCSC Ensembl
chr1:25461733..25499919hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3838187
hg1938187
hg1838187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545826, nsv545833, nsv545830
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv200n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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