A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675686



Internal ID9595105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21651521..22710843hg38UCSC Ensembl
chr17:21552001..22210170hg19UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg381059323
hg19658170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv539e199
Supporting Variantsessv6463181, essv5677382
SamplesHG00311, NA19713
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675686
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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