A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4922n54



Internal ID20138346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15025750..15099845hg38UCSC Ensembl
chr16:15119607..15193702hg19UCSC Ensembl
chr16:15027108..15101203hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3874096
hg1974096
hg1874096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571529, nsv571526, nsv571528
Samples
Known GenesNTAN1, PDXDC1, RRN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4922n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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