A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3593n54



Internal ID22771488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27554600..27626617hg38UCSC Ensembl
chr14:28023806..28095823hg19UCSC Ensembl
chr14:27093646..27165663hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3872018
hg1972018
hg1872018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564130, nsv564132
Samples1787431198_A
Known GenesLINC00645
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3593n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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