A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv516e199



Internal ID20123818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88495803..88498222hg38UCSC Ensembl
chr16:88562211..88564630hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg382420
hg192420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2663469, esv2659592
SamplesNA18907
Known GenesZFPM1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv516e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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