A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1545620



Internal ID12708741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61340328..61340667hg38UCSC Ensembl
chr11:61107800..61108139hg19UCSC Ensembl
chr11:60864376..60864715hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38340
hg19340
hg18340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4365857
SamplesHuRef
Known GenesDAK
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1545620
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