A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3574757



Internal ID6699453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132213725..132214038hg38UCSC Ensembl
chr11:132083619..132083932hg19UCSC Ensembl
chr11:131588829..131589142hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38314
hg19314
hg18314
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv993815
Supporting Variants
SamplesHuRef
Known GenesNTM
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3574757
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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