A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892869



Internal ID19183689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60543296..60584144hg38UCSC Ensembl
Outerchr16:60530184..60584144hg38UCSC Ensembl
Innerchr16:60577200..60618048hg19UCSC Ensembl
Outerchr16:60564088..60618048hg19UCSC Ensembl
Innerchr16:59134701..59175549hg18UCSC Ensembl
Outerchr16:59121589..59175549hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3853961
hg1953961
hg1853961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786115, essv25780859
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892869
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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