A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5806260



Internal ID8783663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21651521..22709465hg38UCSC Ensembl
chr17:21550647..22208792hg19UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg381057945
hg19658146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659416
Supporting Variants
SamplesHG00595
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5806260
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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