A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1050816



Internal ID11867255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112514280..112514833hg38UCSC Ensembl
chr9:115276560..115277113hg19UCSC Ensembl
chr9:114316381..114316934hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38554
hg19554
hg18554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3710310
SamplesHuRef
Known GenesKIAA1958
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1050816
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