A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669181



Internal ID9588600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:97932521..97933164hg38UCSC Ensembl
Outerchr14:97932487..97933199hg38UCSC Ensembl
Innerchr14:98398858..98399501hg19UCSC Ensembl
Outerchr14:98398824..98399536hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38713
hg19713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6182690
SamplesNA19060
Known GenesC14orf64
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669181
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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