A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15555138



Internal ID818051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87555289..87563715hg38UCSC Ensembl
chr16:87588895..87597321hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg388427
hg198427
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639516
Supporting Variants
SamplesHG00406
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15555138
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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