A curated catalogue of human genomic structural variation




Variant Details

Variant: esv993873



Internal ID7078864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:75379921..75382908hg38UCSC Ensembl
Outerchr11:75090965..75093952hg19UCSC Ensembl
Outerchr11:74768613..74771600hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382988
hg192988
hg182988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565737
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv993873
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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