A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626669



Internal ID7013501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65023467..65037106hg38UCSC Ensembl
Innerchr11:65023617..65036956hg38UCSC Ensembl
Outerchr11:65023317..65037256hg38UCSC Ensembl
chr11:64790939..64804578hg19UCSC Ensembl
Innerchr11:64791089..64804428hg19UCSC Ensembl
Outerchr11:64790789..64804728hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3813640
hg1913640
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14189735
SamplesHG01356
Known GenesARL2-SNX15, SNX15
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626669
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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