A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799419



Internal ID19166157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63269405..63559278hg38UCSC Ensembl
Innerchr16:63303309..63593182hg19UCSC Ensembl
Innerchr16:61860810..62150683hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38289874
hg19289874
hg18289874
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892870
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=49
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799419
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