A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3579732



Internal ID7051114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1607735..1607821hg38UCSC Ensembl
chr11:1628965..1629051hg19UCSC Ensembl
chr11:1585541..1585627hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3887
hg1987
hg1887
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv991273
Supporting Variants
SamplesHuRef
Known GenesKRTAP5-3, MOB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3579732
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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