A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv377n54



Internal ID22768272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97818298..97883329hg38UCSC Ensembl
chr1:98283854..98348885hg19UCSC Ensembl
chr1:98056442..98121473hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3865032
hg1965032
hg1865032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv546872, nsv546873
SamplesNINDS_199
Known GenesDPYD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv377n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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