A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3991n54



Internal ID22771886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105472502..105480505hg38UCSC Ensembl
chr14:105938839..105946842hg19UCSC Ensembl
chr14:105009884..105017887hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg388004
hg198004
hg188004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566266, nsv566222, nsv566236
Samples
Known GenesCRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3991n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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