A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3916n54



Internal ID22771811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101457469..101458698hg38UCSC Ensembl
chr14:101923806..101925035hg19UCSC Ensembl
chr14:100993559..100994788hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381230
hg191230
hg181230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565865, nsv565864, nsv565872
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3916n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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