A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3561418



Internal ID18762494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:7305389..7305631hg38UCSC Ensembl
Outerchr3:7305325..7305667hg38UCSC Ensembl
Innerchr3:7347076..7347318hg19UCSC Ensembl
Outerchr3:7347012..7347354hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9760165
Samples
Known GenesGRM7
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3561418
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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