A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9741279



Internal ID18368839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:141414093..141414379hg38UCSC Ensembl
Outerchr7:141414046..141414434hg38UCSC Ensembl
Innerchr7:141113893..141114179hg19UCSC Ensembl
Outerchr7:141113846..141114234hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3542532
Supporting Variants
Samples
Known GenesTMEM178B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9741279
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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