A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637921



Internal ID6678020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11008854..11012240hg38UCSC Ensembl
chr16:11102711..11106097hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg383387
hg193387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15375165, essv15375168, essv15375164, essv15375169, essv15375160, essv15375161, essv15375162, essv15375167, essv15375166, essv15375163
SamplesNA18559, HG00593, HG02397, HG04153, HG00436, HG04141, NA18749, HG03132, NA18631, NA18533
Known GenesCLEC16A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637921
Frequency
Sample Size2504
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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