A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1004439



Internal ID7069536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:61199065..61239863hg38UCSC Ensembl
Outerchr11:60966537..61007335hg19UCSC Ensembl
Outerchr11:60723113..60763911hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3840799
hg1940799
hg1840799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565409
SamplesHuRef
Known GenesPGA3, PGA4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1004439
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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