A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781609



Internal ID19175410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28621186..28659108hg38UCSC Ensembl
Innerchr5:28621293..28659215hg19UCSC Ensembl
Innerchr5:28657050..28694972hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3837923
hg1937923
hg1837923
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894159
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781609
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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