A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665914



Internal ID9932019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34615014..34615631hg38UCSC Ensembl
chr8:34472532..34473149hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38618
hg19618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6326771, essv6427588, essv5813745
SamplesNA19315, NA19401, NA19108
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665914
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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