A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15528229



Internal ID5530045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77166834..77194282hg38UCSC Ensembl
chr16:77200731..77228179hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3827449
hg1927449
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639162
Supporting Variants
SamplesHG00590
Known GenesMON1B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15528229
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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