A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4157925



Internal ID11093778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128585076..128585177hg38UCSC Ensembl
chr11:128454971..128455072hg19UCSC Ensembl
chr11:127960181..127960282hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38102
hg19102
hg18102
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1237588
Supporting Variants
SamplesHuRef
Known GenesETS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4157925
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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