A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3910836



Internal ID11504349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14160563..14160649hg38UCSC Ensembl
chr11:14182109..14182195hg19UCSC Ensembl
chr11:14138685..14138771hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3887
hg1987
hg1887
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1173943
Supporting Variants
SamplesHuRef
Known GenesSPON1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3910836
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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