A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4326592



Internal ID11262444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130091051..130091376hg38UCSC Ensembl
chr11:129960946..129961271hg19UCSC Ensembl
chr11:129466156..129466481hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38326
hg19326
hg18326
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1620466
Supporting Variants
SamplesHuRef
Known GenesAPLP2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4326592
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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