A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3808377



Internal ID11953494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:115095501..115095713hg38UCSC Ensembl
chr9:117857780..117857992hg19UCSC Ensembl
chr9:116897601..116897813hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38213
hg19213
hg18213
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1713245
Supporting Variants
SamplesHuRef
Known GenesTNC
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3808377
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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