A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1000791



Internal ID7065921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:59457161..59464073hg38UCSC Ensembl
Outerchr16:59491065..59497977hg19UCSC Ensembl
Outerchr16:58048566..58055478hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg386913
hg196913
hg186913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564097
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1000791
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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