A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15271566



Internal ID5273382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64165039..64173673hg38UCSC Ensembl
chr15:64457238..64465872hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg388635
hg198635
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636730
Supporting Variants
SamplesNA20862
Known GenesCSNK1G1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15271566
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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