A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15261108



Internal ID5262924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59635720..59677766hg38UCSC Ensembl
chr15:59927919..59969965hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3842047
hg1942047
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636646
Supporting Variants
SamplesHG04210
Known GenesBNIP2, GTF2A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15261108
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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