A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1660982



Internal ID12477414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18597110..18598443hg38UCSC Ensembl
chr8:18454620..18455953hg19UCSC Ensembl
chr8:18498900..18500233hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381334
hg191334
hg181334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4320021
SamplesHuRef
Known GenesPSD3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1660982
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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