A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6504543



Internal ID9481946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21651521..22709157hg38UCSC Ensembl
chr17:21550333..22208484hg19UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg381057637
hg19658152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672459
Supporting Variants
SamplesHG01072
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6504543
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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