A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781222



Internal ID19174818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12462741..12634730hg38UCSC Ensembl
Innerchr16:12556598..12728587hg19UCSC Ensembl
Innerchr16:12464099..12636088hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38171990
hg19171990
hg18171990
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892793
Supporting Variants
Samples
Known GenesSNX29
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=139
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781222
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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