A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676416



Internal ID9942521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:71141868..71146423hg38UCSC Ensembl
Outerchr14:71141711..71146576hg38UCSC Ensembl
Innerchr14:71608585..71613140hg19UCSC Ensembl
Outerchr14:71608428..71613293hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg384866
hg194866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6120178
SamplesHG01440
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676416
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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