A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636621



Internal ID7023415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58095010..58125126hg38UCSC Ensembl
chr15:58387209..58417325hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3830117
hg1930117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15260043, essv15260041, essv15260044, essv15260042
SamplesHG02784, HG03018, NA18962, NA18537
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636621
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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