A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv210n54



Internal ID20133634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25311762..25333196hg38UCSC Ensembl
chr1:25638253..25659687hg19UCSC Ensembl
chr1:25510840..25532274hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3821435
hg1921435
hg1821435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545868, nsv545870
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv210n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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