A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv426n54



Internal ID20133850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:103612312..103617486hg38UCSC Ensembl
chr1:104154934..104160108hg19UCSC Ensembl
chr1:103956457..103961631hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg385175
hg195175
hg185175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv547082, nsv547081
Samples
Known GenesAMY2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv426n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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