A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762482



Internal ID18736728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39537627..39538227hg38UCSC Ensembl
Outerchr4:39537543..39538256hg38UCSC Ensembl
Innerchr4:39539247..39539847hg19UCSC Ensembl
Outerchr4:39539163..39539876hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38714
hg19714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563735
Supporting Variants
Samples
Known GenesMIR1273H, UGDH-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762482
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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