A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892936



Internal ID18837070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88755889..88764428hg38UCSC Ensembl
Outerchr16:88755889..88764428hg38UCSC Ensembl
Innerchr16:88822297..88830836hg19UCSC Ensembl
Outerchr16:88822297..88830836hg19UCSC Ensembl
Innerchr16:87349798..87358337hg18UCSC Ensembl
Outerchr16:87349798..87358337hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg388540
hg198540
hg188540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798635
Samples
Known GenesPIEZO1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892936
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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