A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010932



Internal ID7074883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:101413118..101423312hg38UCSC Ensembl
Outerchr7:101056399..101066593hg19UCSC Ensembl
Outerchr7:100843119..100853313hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3810195
hg1910195
hg1810195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564417
SamplesHuRef
Known GenesCOL26A1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010932
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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