A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4153758



Internal ID11089610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1874091..1874091hg38UCSC Ensembl
chr11:1895321..1895321hg19UCSC Ensembl
chr11:1851897..1851897hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1740077
Supporting Variants
SamplesHuRef
Known GenesLSP1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4153758
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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