A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666508



Internal ID9585927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21651521..22712031hg38UCSC Ensembl
chr17:21553173..22211358hg19UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg381060511
hg19658186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv539e199
Supporting Variantsessv5795897, essv6576081, essv6014964
SamplesHG00325, NA19462, NA19376
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666508
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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