A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637918



Internal ID6678018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10884011..10887785hg38UCSC Ensembl
Innerchr16:10884021..10887776hg38UCSC Ensembl
Outerchr16:10884002..10887795hg38UCSC Ensembl
chr16:10977868..10981642hg19UCSC Ensembl
Innerchr16:10977878..10981633hg19UCSC Ensembl
Outerchr16:10977859..10981652hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg383775
hg193775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15374109, essv15374110
SamplesHG03916, HG02181
Known GenesCIITA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637918
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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