A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9758326



Internal ID18732572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:98593884..98593936hg38UCSC Ensembl
chr2:99210347..99210399hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559579
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9758326
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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