A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677642



Internal ID9943747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21653363..22715771hg38UCSC Ensembl
chr17:21556985..22215098hg19UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg381062409
hg19658114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv539e199
Supporting Variantsessv6124222
SamplesNA19247
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677642
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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