A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3840n54



Internal ID20137264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87923791..87961245hg38UCSC Ensembl
chr14:88390135..88427589hg19UCSC Ensembl
chr14:87459888..87497342hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3837455
hg1937455
hg1837455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565510, nsv565507, nsv565508, nsv565505, nsv565509
Samples
Known GenesGALC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3840n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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