A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv230e214



Internal ID22756124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107682939..107838250hg38UCSC Ensembl
chr11:107553665..107708976hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38155312
hg19155312
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3627653, esv3627654
SamplesHG03645, HG00238, HG02049, NA19328, NA19468
Known GenesSLC35F2, SLN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv230e214
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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