A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677059



Internal ID9943164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:106219819..106768516hg38UCSC Ensembl
chr14:106676463..107176758hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38548698
hg19500296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv429e199
Supporting Variantsessv6011033
SamplesNA20540
Known GenesLINC00221, LINC00226
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677059
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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