A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv502e214



Internal ID20121925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28841240..28861977hg38UCSC Ensembl
chr16:28852561..28873298hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3820738
hg1920738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3638346, esv3638347
SamplesHG02655
Known GenesMIR4721, TUFM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv502e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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