A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4320701



Internal ID11603239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2856558..2856631hg38UCSC Ensembl
chr11:2877788..2877861hg19UCSC Ensembl
chr11:2834364..2834437hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3874
hg1974
hg1874
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1473398
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4320701
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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