A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628204



Internal ID7015028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134933906..135024674hg38UCSC Ensembl
Innerchr11:134934056..135024524hg38UCSC Ensembl
Outerchr11:134933756..135024824hg38UCSC Ensembl
chr11:134803800..134894568hg19UCSC Ensembl
Innerchr11:134803950..134894418hg19UCSC Ensembl
Outerchr11:134803650..134894718hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3890769
hg1990769
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14326929, essv14326930, essv14326931, essv14326934, essv14326933, essv14326932
SamplesHG03679, HG03897, HG03844, HG03711, HG02790, HG03856
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628204
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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