A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799706



Internal ID19175073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:103341663..103441319hg38UCSC Ensembl
Innerchr5:102677364..102777020hg19UCSC Ensembl
Innerchr5:102705263..102804919hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3899657
hg1999657
hg1899657
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890687
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799706
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer