A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762965



Internal ID18390525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:88760364..88760610hg38UCSC Ensembl
Outerchr4:88760300..88760651hg38UCSC Ensembl
Innerchr4:89681515..89681761hg19UCSC Ensembl
Outerchr4:89681451..89681802hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564218
Supporting Variants
Samples
Known GenesFAM13A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762965
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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