A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3561362



Internal ID18415752
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 StatusM
Merged Variants
Supporting Variantsessv9760109
Samples
Known GenesCNTN4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3561362
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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