A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9741062



Internal ID18368622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:115943590..115947446hg38UCSC Ensembl
Outerchr7:115943447..115947946hg38UCSC Ensembl
Innerchr7:115583644..115587500hg19UCSC Ensembl
Outerchr7:115583501..115588000hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3542315
Supporting Variants
Samples
Known GenesTFEC
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9741062
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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