A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998494



Internal ID6734426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:24811167..24817824hg38UCSC Ensembl
Outerchr6:24811395..24818052hg19UCSC Ensembl
Outerchr6:24919374..24926031hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg386658
hg196658
hg186658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563503
SamplesHuRef
Known GenesFAM65B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998494
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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