A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9743876



Internal ID18718122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92250608..92250677hg38UCSC Ensembl
chr9:95012890..95012959hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545129
Supporting Variants
Samples
Known GenesIARS
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9743876
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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