A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626759



Internal ID7013589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70055959..70057102hg38UCSC Ensembl
Innerchr11:70055961..70057101hg38UCSC Ensembl
Outerchr11:70055958..70057104hg38UCSC Ensembl
chr11:69902065..69903208hg19UCSC Ensembl
Innerchr11:69902067..69903207hg19UCSC Ensembl
Outerchr11:69902064..69903210hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg381144
hg191144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14207086, essv14207085, essv14207099, essv14207095, essv14207091, essv14207094, essv14207097, essv14207093, essv14207092, essv14207090, essv14207087, essv14207098, essv14207096, essv14207088, essv14207089
SamplesHG03139, HG03082, HG03135, NA19138, HG01242, HG02505, HG02009, HG02144, HG02309, HG01896, NA19037, HG00638, NA19439, NA19438, HG02805
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626759
Frequency
Sample Size2504
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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