A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1014341



Internal ID12177468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58050644..58052644hg38UCSC Ensembl
chr11:57818116..57820116hg19UCSC Ensembl
chr11:57574692..57576692hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg382001
hg192001
hg182001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4272343
SamplesHuRef
Known GenesOR9Q1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1014341
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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