A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3785741



Internal ID11976130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38324879..38325285hg38UCSC Ensembl
chr9:38324876..38325282hg19UCSC Ensembl
chr9:38314876..38315282hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38407
hg19407
hg18407
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1248535
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3785741
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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