A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007864



Internal ID7072957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2384503..2384553hg38UCSC Ensembl
chr11:2405733..2405783hg19UCSC Ensembl
chr11:2362309..2362359hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3579795
SamplesHuRef
Known GenesCD81
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007864
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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