A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4919n54



Internal ID20138343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14939348..15040518hg38UCSC Ensembl
chr16:15033205..15134375hg19UCSC Ensembl
chr16:14940706..15041876hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38101171
hg19101171
hg18101171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571524, nsv571517
Samples
Known GenesMIR1972-1, MIR1972-2, NPIPA1, NTAN1, PDXDC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4919n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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