A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656866



Internal ID9922971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:96886574..96897238hg38UCSC Ensembl
Outerchr14:96886417..96897391hg38UCSC Ensembl
Innerchr14:97352911..97363575hg19UCSC Ensembl
Outerchr14:97352754..97363728hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3810975
hg1910975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv411e199
Supporting Variantsessv6364383, essv6370148
SamplesNA18597, NA18562
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656866
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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