A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892960



Internal ID19183780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13384528..13484926hg38UCSC Ensembl
Outerchr17:13384528..13488405hg38UCSC Ensembl
Innerchr17:13287845..13388243hg19UCSC Ensembl
Outerchr17:13287845..13391722hg19UCSC Ensembl
Innerchr17:13228570..13328968hg18UCSC Ensembl
Outerchr17:13228570..13332447hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38103878
hg19103878
hg18103878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779649, essv25797886, essv25800118, essv25798102, essv25797877
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892960
Frequency
Sample Size3017
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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