A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3542479



Internal ID18743555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135904408..135904666hg38UCSC Ensembl
Outerchr7:135904394..135904667hg38UCSC Ensembl
Innerchr7:135589156..135589414hg19UCSC Ensembl
Outerchr7:135589142..135589415hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9741226
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3542479
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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