A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5260n54



Internal ID20138684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83994518..84005144hg38UCSC Ensembl
chr16:84028123..84038749hg19UCSC Ensembl
chr16:82585624..82596250hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3810627
hg1910627
hg1810627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573416, nsv573414
SamplesHGDP00784, 1780854206_A
Known GenesNECAB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5260n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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