A curated catalogue of human genomic structural variation




Variant Details

Variant: esv999969



Internal ID7082577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:66392056..66396323hg38UCSC Ensembl
Outerchr7:65857043..65861310hg19UCSC Ensembl
Outerchr7:65494478..65498745hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg384268
hg194268
hg184268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565624
SamplesHuRef
Known GenesLINC00174
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv999969
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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