A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676639



Internal ID9942744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13415332..13415597hg38UCSC Ensembl
chr17:13318649..13318914hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5563587, essv5816088
SamplesNA19703, NA19311
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676639
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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