A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641058



Internal ID7027832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:66280778..66283826hg38UCSC Ensembl
chr17:64276896..64279944hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg383049
hg193049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv584e214
Supporting Variantsessv15725033, essv15725036, essv15725032, essv15725030, essv15725037, essv15725034, essv15725035, essv15725031
SamplesNA21089, HG04018, HG03943, HG03007, HG04039, HG04107, HG04235, HG04080
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641058
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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