A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892963



Internal ID19183783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15093691..15131524hg38UCSC Ensembl
Outerchr17:15091369..15151510hg38UCSC Ensembl
Innerchr17:14997008..15034841hg19UCSC Ensembl
Outerchr17:14994686..15054827hg19UCSC Ensembl
Innerchr17:14937733..14975566hg18UCSC Ensembl
Outerchr17:14935411..14995552hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3860142
hg1960142
hg1860142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781403, essv25779535, essv25785010, essv25784359, essv25798398, essv25779465, essv25800232, essv25801293, essv25782016, essv25779177, essv25779694, essv25783594, essv25785256, essv25796056, essv25784288, essv25783682
Samples
Known GenesCDRT8
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892963
Frequency
Sample Size3017
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer