A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627654



Internal ID6667801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107701579..107838250hg38UCSC Ensembl
chr11:107572305..107708976hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38136672
hg19136672
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv230e214
Supporting Variantsessv14276850, essv14276849, essv14276851
SamplesHG03645, HG00238, HG02049
Known GenesSLC35F2, SLN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627654
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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