A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3566859



Internal ID6691555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131928564..131928661hg38UCSC Ensembl
chr11:131798458..131798555hg19UCSC Ensembl
chr11:131303668..131303765hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3898
hg1998
hg1898
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1008024
Supporting Variants
SamplesHuRef
Known GenesNTM
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3566859
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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