A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625367



Internal ID7012201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10942933..10964251hg38UCSC Ensembl
Innerchr11:10943083..10964101hg38UCSC Ensembl
Outerchr11:10942783..10964401hg38UCSC Ensembl
chr11:10964480..10985798hg19UCSC Ensembl
Innerchr11:10964630..10985648hg19UCSC Ensembl
Outerchr11:10964330..10985948hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3821319
hg1921319
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv185e214
Supporting Variantsessv14029109, essv14029104, essv14029106, essv14029105, essv14029107, essv14029116, essv14029112, essv14029113, essv14029117, essv14029115, essv14029108, essv14029118, essv14029114, essv14029119, essv14029103, essv14029111, essv14029110
SamplesHG00142, HG03517, NA19171, NA19131, HG00610, HG00182, HG03267, NA19209, HG02009, HG03363, NA19440, NA19331, NA19334, NA19428, HG03157, NA20334, HG00628
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625367
Frequency
Sample Size2504
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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