A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626609



Internal ID6666759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62493573..62494981hg38UCSC Ensembl
Innerchr11:62493580..62494975hg38UCSC Ensembl
Outerchr11:62493567..62494988hg38UCSC Ensembl
chr11:62261045..62262453hg19UCSC Ensembl
Innerchr11:62261052..62262447hg19UCSC Ensembl
Outerchr11:62261039..62262460hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381409
hg191409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14179715, essv14179716, essv14179712, essv14179709, essv14179706, essv14179714, essv14179704, essv14179703, essv14179718, essv14179710, essv14179711, essv14179713, essv14179708, essv14179717, essv14179707, essv14179705
SamplesNA19020, NA18504, NA19107, NA19198, NA19347, HG02511, NA18915, HG03159, HG03202, HG02309, NA19376, HG02971, NA19102, HG02855, NA18511, HG03265
Known GenesAHNAK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626609
Frequency
Sample Size2504
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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