A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663045



Internal ID9929150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38740243..38744491hg38UCSC Ensembl
Outerchr14:38740086..38744644hg38UCSC Ensembl
Innerchr14:39209447..39213695hg19UCSC Ensembl
Outerchr14:39209290..39213848hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg384559
hg194559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6441040
SamplesHG00708
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663045
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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