A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662870



Internal ID9928975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:71468899..71469124hg38UCSC Ensembl
Outerchr14:71468862..71469174hg38UCSC Ensembl
Innerchr14:71935616..71935841hg19UCSC Ensembl
Outerchr14:71935579..71935891hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5741271
SamplesHG00310
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662870
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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