A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4099511



Internal ID11662364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128868092..128868092hg38UCSC Ensembl
chr11:128737987..128737987hg19UCSC Ensembl
chr11:128243197..128243197hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382307
hg192307
hg182307
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1649942
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4099511
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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