A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv409n54



Internal ID22768304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:103599256..103618188hg38UCSC Ensembl
chr1:104141878..104160810hg19UCSC Ensembl
chr1:103943401..103962333hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3818933
hg1918933
hg1818933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv547018, nsv547020, nsv547019, nsv547021
Samples
Known GenesAMY2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv409n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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