A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892925



Internal ID19183745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84022293..84049179hg38UCSC Ensembl
Outerchr16:84022293..84049179hg38UCSC Ensembl
Innerchr16:84055898..84082784hg19UCSC Ensembl
Outerchr16:84055898..84082784hg19UCSC Ensembl
Innerchr16:82613399..82640285hg18UCSC Ensembl
Outerchr16:82613399..82640285hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3826887
hg1926887
hg1826887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785440
Samples
Known GenesSLC38A8
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892925
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