A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669759



Internal ID9589178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21651521..22708983hg38UCSC Ensembl
chr17:21550164..22208310hg19UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg381057463
hg19658147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv539e199
Supporting Variantsessv5620658, essv6177134
SamplesNA19704, NA19663
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669759
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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