A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3541802



Internal ID18742878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66392773..66395100hg38UCSC Ensembl
Outerchr7:66392418..66395286hg38UCSC Ensembl
Innerchr7:65857760..65860087hg19UCSC Ensembl
Outerchr7:65857405..65860273hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg382869
hg192869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9740549
Samples
Known GenesLINC00174
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3541802
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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