A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9763726



Internal ID18391286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169178281..169178333hg38UCSC Ensembl
chr4:170099432..170099484hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564979
Supporting Variants
Samples
Known GenesSH3RF1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9763726
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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