A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010089



Internal ID7074154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:118130766..118133851hg38UCSC Ensembl
Outerchr6:118451929..118455014hg19UCSC Ensembl
Outerchr6:118558622..118561707hg18UCSC Ensembl
Cytoband6q22.2
Allele length
AssemblyAllele length
hg383086
hg193086
hg183086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565044
SamplesHuRef
Known GenesSLC35F1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010089
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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