A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637967



Internal ID6678066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12666471..12685176hg38UCSC Ensembl
Innerchr16:12666471..12685176hg38UCSC Ensembl
Outerchr16:12665971..12685676hg38UCSC Ensembl
chr16:12760328..12779033hg19UCSC Ensembl
Innerchr16:12760328..12779033hg19UCSC Ensembl
Outerchr16:12759828..12779533hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3818706
hg1918706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15377493
SamplesHG03756
Known GenesCPPED1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637967
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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