A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762150



Internal ID18389710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9955207..9955494hg38UCSC Ensembl
Outerchr4:9955113..9955568hg38UCSC Ensembl
Innerchr4:9956831..9957118hg19UCSC Ensembl
Outerchr4:9956737..9957192hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563403
Supporting Variants
Samples
Known GenesSLC2A9
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762150
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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