A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv209n54



Internal ID18992385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25307714..25338308hg38UCSC Ensembl
chr1:25634205..25664799hg19UCSC Ensembl
chr1:25506792..25537386hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3830595
hg1930595
hg1830595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545869, nsv545866, nsv545871, nsv545867
Samples
Known GenesRHD, TMEM50A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv209n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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