A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9760109



Internal ID18387669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2980334..2980427hg38UCSC Ensembl
chr3:3022018..3022111hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3561362
Supporting Variants
Samples
Known GenesCNTN4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9760109
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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