A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892861



Internal ID18836995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:53664764..53756994hg38UCSC Ensembl
Outerchr16:53664764..53756994hg38UCSC Ensembl
Innerchr16:53698676..53790906hg19UCSC Ensembl
Outerchr16:53698676..53790906hg19UCSC Ensembl
Innerchr16:52256177..52348407hg18UCSC Ensembl
Outerchr16:52256177..52348407hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3892231
hg1992231
hg1892231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785889
Samples
Known GenesFTO, RPGRIP1L
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892861
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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