A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3289051



Internal ID10962031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:666376..667821hg38UCSC Ensembl
Outerchr6:666376..667821hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381446
hg191446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7558618
SamplesHuRef
Known GenesEXOC2
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3289051
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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