A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6230168



Internal ID9462890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:106233354..106773460hg38UCSC Ensembl
chr14:106689963..107181699hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38540107
hg19491737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671687
Supporting Variants
SamplesNA18916
Known GenesLINC00221, LINC00226
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6230168
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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