A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9763471



Internal ID18737717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:140712159..140712449hg38UCSC Ensembl
Outerchr4:140712153..140712455hg38UCSC Ensembl
Innerchr4:141633313..141633603hg19UCSC Ensembl
Outerchr4:141633307..141633609hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564724
Supporting Variants
Samples
Known GenesTBC1D9
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9763471
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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