A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010000



Internal ID7059694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:31482058..31493451hg38UCSC Ensembl
Outerchr7:31521672..31533065hg19UCSC Ensembl
Outerchr7:31488197..31499590hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3811394
hg1911394
hg1811394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564806
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010000
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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