A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3287829



Internal ID10960809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:24811659..24817734hg38UCSC Ensembl
Outerchr6:24811887..24817962hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386076
hg196076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7557396
SamplesHuRef
Known GenesFAM65B
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3287829
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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