A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3889382



Internal ID11872489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1684572..1684891hg38UCSC Ensembl
chr11:1705802..1706121hg19UCSC Ensembl
chr11:1662378..1662697hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38320
hg19320
hg18320
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1323796
Supporting Variants
SamplesHuRef
Known GenesFAM99B, MOB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3889382
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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