A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636896



Internal ID6677003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73818723..73875766hg38UCSC Ensembl
chr15:74111064..74168107hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3857044
hg1957044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15292637, essv15292636
SamplesHG01705, HG01516
Known GenesTBC1D21
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636896
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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