A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008506



Internal ID7073483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:2819373..2824235hg38UCSC Ensembl
Outerchr6:2819607..2824469hg19UCSC Ensembl
Outerchr6:2764606..2769468hg18UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg384863
hg194863
hg184863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564330
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008506
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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