A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637959



Internal ID7024746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12351614..12368675hg38UCSC Ensembl
chr16:12445471..12462532hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3817062
hg1917062
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15377432
SamplesHG02108
Known GenesSNX29
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637959
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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