A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661628



Internal ID9581047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106344349..106867592hg38UCSC Ensembl
Outerchr14:106344316..106867627hg38UCSC Ensembl
Innerchr14:106800273..107275805hg19UCSC Ensembl
Outerchr14:106800239..107275840hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38523312
hg19475602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5429602
SamplesNA19909
Known GenesLINC00221
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661628
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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