A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3683306



Internal ID12078563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56703102..56703102hg38UCSC Ensembl
chr11:56470578..56470578hg19UCSC Ensembl
chr11:56227154..56227154hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3811069
hg1911069
hg1811069
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1365554
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3683306
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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