A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1135936



Internal ID12299059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9083003..9083003hg38UCSC Ensembl
chr11:9104550..9104550hg19UCSC Ensembl
chr11:9061126..9061126hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382264
hg192264
hg182264
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4284468
SamplesHuRef
Known GenesSCUBE2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1135936
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer