A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv201n54



Internal ID18992377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25262655..25339480hg38UCSC Ensembl
chr1:25589146..25665971hg19UCSC Ensembl
chr1:25461733..25538558hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3876826
hg1976826
hg1876826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545840, nsv545838, nsv545827, nsv545841, nsv545839, nsv545828, nsv545831, nsv545842
Samples
Known GenesRHD, TMEM50A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv201n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss44
Observed Complex0
Frequencyn/a


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